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LBG00ukk:R:16402BC01:CBZ1Sk013 - Revision history
2026-06-16T14:15:20Z
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<p><a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013:01" class="mw-redirect" title="LBG00ukk:R:16402BC01:CBZ1Sk013:01">LBG00ukk:R:16402BC01:CBZ1Sk013:01</a> moved to <a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013" title="LBG00ukk:R:16402BC01:CBZ1Sk013">LBG00ukk:R:16402BC01:CBZ1Sk013</a></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 06:00, 15 April 2010</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&& (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol&&</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&&(S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol&&</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[ alpha ]^{25}_D =-2.4° (C3.2, CHCl_3 )<<0174>></div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[ alpha ]^{25}_D =-2.4° (C3.2, CHCl_3 )<<0174>></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<<0174>>, </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<<0174>>, </div></td></tr>
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Editor: LBG00ukk:R:16402BC01:CBZ1Sk013:01 moved to LBG00ukk:R:16402BC01:CBZ1Sk013
2010-02-25T10:00:10Z
<p><a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013:01" class="mw-redirect" title="LBG00ukk:R:16402BC01:CBZ1Sk013:01">LBG00ukk:R:16402BC01:CBZ1Sk013:01</a> moved to <a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013" title="LBG00ukk:R:16402BC01:CBZ1Sk013">LBG00ukk:R:16402BC01:CBZ1Sk013</a></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 19:00, 25 February 2010</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l5">Line 5:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&& (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol&&</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&& (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol&&</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[ alpha ]^<del style="font-weight: bold; text-decoration: none;">25_D </del>=-2.4° (C3.2, CHCl_3 )<<0174>></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[ alpha ]^<ins style="font-weight: bold; text-decoration: none;">{25}_D </ins>=-2.4° (C3.2, CHCl_3 )<<0174>></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<<0174>>, </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<<0174>>, </div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H NMR (300MHz,CDCl_3 ) 0.1(6H, s, 2CH_3 on Si), 0.9(9H, s, 3CH_3 on tert-butyl), 1.55-1.7(15H, m, 5CH_3 on geranylgeranyl), 1.95-3.15(12H, br m, 6CH_2 on geranylgeranyl), 3.45-3.70(5H, br m), 4.18[2H, d, J=6.7Hz H at C(1) on geranylgeranyl], 4.58(2H, s, CH_2 ), 5.0-5.2[3H m, H at C(6), C(10) and C(14)], 5.4 [1H, t, J=6.7Hz H at C(2) on geranylgeranyl], 7.25(5H, br m)<BR>^<del style="font-weight: bold; text-decoration: none;">1 ^3 </del>C NMR(75MHz, CDCl_3 )-5,2(q), 16.0(q), 16.5(q), 17.7(q), 18.2(q), 18.5(s), 25.2(q), 25.9(q), 26.37(t), 26.44(t), 27.8(t), 39.6(t), 39.7(t), 63.0(t), 66.9(t), 70.2(t), 73.5(t), 78.5(d), 121.2(d), 123.9(d), 124.2(d), 124.4(d), 127.46(d), 127.50(d), 128.3(d), 128.5(s), 132.0(s), 134.9(s), 135.2(s), 139.7(s)<<0174>>, </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H NMR (300MHz,CDCl_3 ) 0.1(6H, s, 2CH_3 on Si), 0.9(9H, s, 3CH_3 on tert-butyl), 1.55-1.7(15H, m, 5CH_3 on geranylgeranyl), 1.95-3.15(12H, br m, 6CH_2 on geranylgeranyl), 3.45-3.70(5H, br m), 4.18[2H, d, J=6.7Hz H at C(1) on geranylgeranyl], 4.58(2H, s, CH_2 ), 5.0-5.2[3H m, H at C(6), C(10) and C(14)], 5.4 [1H, t, J=6.7Hz H at C(2) on geranylgeranyl], 7.25(5H, br m)<BR>^<ins style="font-weight: bold; text-decoration: none;">{13}</ins>C NMR(75MHz, CDCl_3 )-5,2(q), 16.0(q), 16.5(q), 17.7(q), 18.2(q), 18.5(s), 25.2(q), 25.9(q), 26.37(t), 26.44(t), 27.8(t), 39.6(t), 39.7(t), 63.0(t), 66.9(t), 70.2(t), 73.5(t), 78.5(d), 121.2(d), 123.9(d), 124.2(d), 124.4(d), 127.46(d), 127.50(d), 128.3(d), 128.5(s), 132.0(s), 134.9(s), 135.2(s), 139.7(s)<<0174>>, </div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chromatograms=chromatography on silica (Rf=0.57, ethyl acetate-hexane(2:23) )<<0174>>, </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chromatograms=chromatography on silica (Rf=0.57, ethyl acetate-hexane(2:23) )<<0174>>, </div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Lipid/Footer}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Lipid/Footer}}</div></td></tr>
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<p><a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013:01" class="mw-redirect" title="LBG00ukk:R:16402BC01:CBZ1Sk013:01">LBG00ukk:R:16402BC01:CBZ1Sk013:01</a> moved to <a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013" title="LBG00ukk:R:16402BC01:CBZ1Sk013">LBG00ukk:R:16402BC01:CBZ1Sk013</a></p>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&& (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol&&</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&& (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol&&</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[alpha]^25_D =-2.4° (C3.2, CHCl_3 )<<0174>></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[ alpha ]^25_D =-2.4° (C3.2, CHCl_3 )<<0174>></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<<0174>>, </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<<0174>>, </div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H NMR (300MHz,CDCl_3 ) 0.1(6H, s, 2CH_3 on Si), 0.9(9H, s, 3CH_3 on tert-butyl), 1.55-1.7(15H, m, 5CH_3 on geranylgeranyl), 1.95-3.15(12H, br m, 6CH_2 on geranylgeranyl), 3.45-3.70(5H, br m), 4.18[2H, d, J=6.7Hz H at C(1) on geranylgeranyl], 4.58(2H, s, CH_2 ), 5.0-5.2[3H m, H at C(6), C(10) and C(14)], 5.4 [1H, t, J=6.7Hz H at C(2) on geranylgeranyl], 7.25(5H, br m)<BR>^1 ^3 C NMR(75MHz, CDCl_3 )-5,2(q), 16.0(q), 16.5(q), 17.7(q), 18.2(q), 18.5(s), 25.2(q), 25.9(q), 26.37(t), 26.44(t), 27.8(t), 39.6(t), 39.7(t), 63.0(t), 66.9(t), 70.2(t), 73.5(t), 78.5(d), 121.2(d), 123.9(d), 124.2(d), 124.4(d), 127.46(d), 127.50(d), 128.3(d), 128.5(s), 132.0(s), 134.9(s), 135.2(s), 139.7(s)<<0174>>, </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=^1 H NMR (300MHz,CDCl_3 ) 0.1(6H, s, 2CH_3 on Si), 0.9(9H, s, 3CH_3 on tert-butyl), 1.55-1.7(15H, m, 5CH_3 on geranylgeranyl), 1.95-3.15(12H, br m, 6CH_2 on geranylgeranyl), 3.45-3.70(5H, br m), 4.18[2H, d, J=6.7Hz H at C(1) on geranylgeranyl], 4.58(2H, s, CH_2 ), 5.0-5.2[3H m, H at C(6), C(10) and C(14)], 5.4 [1H, t, J=6.7Hz H at C(2) on geranylgeranyl], 7.25(5H, br m)<BR>^1 ^3 C NMR(75MHz, CDCl_3 )-5,2(q), 16.0(q), 16.5(q), 17.7(q), 18.2(q), 18.5(s), 25.2(q), 25.9(q), 26.37(t), 26.44(t), 27.8(t), 39.6(t), 39.7(t), 63.0(t), 66.9(t), 70.2(t), 73.5(t), 78.5(d), 121.2(d), 123.9(d), 124.2(d), 124.4(d), 127.46(d), 127.50(d), 128.3(d), 128.5(s), 132.0(s), 134.9(s), 135.2(s), 139.7(s)<<0174>>, </div></td></tr>
</table>
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Editor: LBG00ukk:R:16402BC01:CBZ1Sk013:01 moved to LBG00ukk:R:16402BC01:CBZ1Sk013
2010-02-19T14:00:00Z
<p><a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013:01" class="mw-redirect" title="LBG00ukk:R:16402BC01:CBZ1Sk013:01">LBG00ukk:R:16402BC01:CBZ1Sk013:01</a> moved to <a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013" title="LBG00ukk:R:16402BC01:CBZ1Sk013">LBG00ukk:R:16402BC01:CBZ1Sk013</a></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
<col class="diff-marker" />
<col class="diff-content" />
<col class="diff-marker" />
<col class="diff-content" />
<tr class="diff-title" lang="en">
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 23:00, 19 February 2010</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l5">Line 5:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&& (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol&&</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=&& (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol&&</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[<del style="font-weight: bold; text-decoration: none;"><FONT FACE="Symbol">a</FONT></del>]<del style="font-weight: bold; text-decoration: none;"><sub>D</sub><sup>25</sup></del>=-2.4° (C3.2, <del style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT SIZE=-1>3</FONT></SUB></del>)<<0174>></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[<ins style="font-weight: bold; text-decoration: none;">alpha</ins>]<ins style="font-weight: bold; text-decoration: none;">^25_D </ins>=-2.4° (C3.2, <ins style="font-weight: bold; text-decoration: none;">CHCl_3 </ins>)<<0174>></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<<0174>>, </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<<0174>>, </div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=<del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=-1></del>1<del style="font-weight: bold; text-decoration: none;"></FONT></SUP></del>H NMR (300MHz,<del style="font-weight: bold; text-decoration: none;">CDCl<SUB><FONT SIZE=-1>3</FONT></SUB></del>) 0.1(6H, s, <del style="font-weight: bold; text-decoration: none;">2CH<SUB><FONT SIZE=-1>3</FONT></SUB> </del>on Si), 0.9(9H, s, <del style="font-weight: bold; text-decoration: none;">3CH<SUB><FONT SIZE=-1>3</FONT></SUB> </del>on tert-butyl), 1.55-1.7(15H, m, <del style="font-weight: bold; text-decoration: none;">5CH<SUB><FONT SIZE=-1>3</FONT></SUB> </del>on geranylgeranyl), 1.95-3.15(12H, br m, <del style="font-weight: bold; text-decoration: none;">6CH<SUB><FONT SIZE=-1>2</FONT></SUB> </del>on geranylgeranyl), 3.45-3.70(5H, br m), 4.18[2H, d, J=6.7Hz H at C(1) on geranylgeranyl], 4.58(2H, s, <del style="font-weight: bold; text-decoration: none;">CH<SUB><FONT SIZE=-1>2</FONT></SUB></del>), 5.0-5.2[3H m, H at C(6), C(10) and C(14)], 5.4 [1H, t, J=6.7Hz H at C(2) on geranylgeranyl], 7.25(5H, br m)<BR><del style="font-weight: bold; text-decoration: none;"><SUP><FONT SIZE=-1></del>1<del style="font-weight: bold; text-decoration: none;"></FONT></SUP><SUP><FONT SIZE=-1></del>3<del style="font-weight: bold; text-decoration: none;"></FONT></SUP></del>C NMR(75MHz, <del style="font-weight: bold; text-decoration: none;">CDCl<SUB><FONT SIZE=-1>3</FONT></SUB></del>)-5,2(q), 16.0(q), 16.5(q), 17.7(q), 18.2(q), 18.5(s), 25.2(q), 25.9(q), 26.37(t), 26.44(t), 27.8(t), 39.6(t), 39.7(t), 63.0(t), 66.9(t), 70.2(t), 73.5(t), 78.5(d), 121.2(d), 123.9(d), 124.2(d), 124.4(d), 127.46(d), 127.50(d), 128.3(d), 128.5(s), 132.0(s), 134.9(s), 135.2(s), 139.7(s)<<0174>>, </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=<ins style="font-weight: bold; text-decoration: none;">^</ins>1 H NMR (300MHz,<ins style="font-weight: bold; text-decoration: none;">CDCl_3 </ins>) 0.1(6H, s, <ins style="font-weight: bold; text-decoration: none;">2CH_3 </ins>on Si), 0.9(9H, s, <ins style="font-weight: bold; text-decoration: none;">3CH_3 </ins>on tert-butyl), 1.55-1.7(15H, m, <ins style="font-weight: bold; text-decoration: none;">5CH_3 </ins>on geranylgeranyl), 1.95-3.15(12H, br m, <ins style="font-weight: bold; text-decoration: none;">6CH_2 </ins>on geranylgeranyl), 3.45-3.70(5H, br m), 4.18[2H, d, J=6.7Hz H at C(1) on geranylgeranyl], 4.58(2H, s, <ins style="font-weight: bold; text-decoration: none;">CH_2 </ins>), 5.0-5.2[3H m, H at C(6), C(10) and C(14)], 5.4 [1H, t, J=6.7Hz H at C(2) on geranylgeranyl], 7.25(5H, br m)<BR><ins style="font-weight: bold; text-decoration: none;">^</ins>1 <ins style="font-weight: bold; text-decoration: none;">^</ins>3 C NMR(75MHz, <ins style="font-weight: bold; text-decoration: none;">CDCl_3 </ins>)-5,2(q), 16.0(q), 16.5(q), 17.7(q), 18.2(q), 18.5(s), 25.2(q), 25.9(q), 26.37(t), 26.44(t), 27.8(t), 39.6(t), 39.7(t), 63.0(t), 66.9(t), 70.2(t), 73.5(t), 78.5(d), 121.2(d), 123.9(d), 124.2(d), 124.4(d), 127.46(d), 127.50(d), 128.3(d), 128.5(s), 132.0(s), 134.9(s), 135.2(s), 139.7(s)<<0174>>, </div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chromatograms=chromatography on silica (Rf=0.57, ethyl acetate-hexane(2:23) )<<0174>>, </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Chromatograms=chromatography on silica (Rf=0.57, ethyl acetate-hexane(2:23) )<<0174>>, </div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td></tr>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Lipid/Footer}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Lipid/Footer}}</div></td></tr>
</table>
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Editor: LBG00ukk:R:16402BC01:CBZ1Sk013:01 moved to LBG00ukk:R:16402BC01:CBZ1Sk013
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<p><a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013:01" class="mw-redirect" title="LBG00ukk:R:16402BC01:CBZ1Sk013:01">LBG00ukk:R:16402BC01:CBZ1Sk013:01</a> moved to <a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013" title="LBG00ukk:R:16402BC01:CBZ1Sk013">LBG00ukk:R:16402BC01:CBZ1Sk013</a></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 00:00, 19 February 2010</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=EEL0209</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=EEL0209</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Common Name= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=<ins style="font-weight: bold; text-decoration: none;">&& </ins>(S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol<ins style="font-weight: bold; text-decoration: none;">&&</ins></div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[FONT FACE=<del style="font-weight: bold; text-decoration: none;">Symbola</del>/FONT]<del style="font-weight: bold; text-decoration: none;">subD</del>/<del style="font-weight: bold; text-decoration: none;">subsup25</del>/sup=-2.4° (C3.2, <del style="font-weight: bold; text-decoration: none;">CHClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB)0174</div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[<ins style="font-weight: bold; text-decoration: none;"><</ins>FONT FACE=<ins style="font-weight: bold; text-decoration: none;">"Symbol">a<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">></ins>]<ins style="font-weight: bold; text-decoration: none;"><sub>D<</ins>/<ins style="font-weight: bold; text-decoration: none;">sub><sup>25<</ins>/sup<ins style="font-weight: bold; text-decoration: none;">></ins>=-2.4° (C3.2, <ins style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>3<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">></ins>)<ins style="font-weight: bold; text-decoration: none;"><<</ins>0174<ins style="font-weight: bold; text-decoration: none;">>></ins></div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)0174, </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<ins style="font-weight: bold; text-decoration: none;"><<</ins>0174<ins style="font-weight: bold; text-decoration: none;">>></ins>, </div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=<del style="font-weight: bold; text-decoration: none;">SUPFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">11</del>/FONT/<del style="font-weight: bold; text-decoration: none;">SUPH </del>NMR (300MHz,<del style="font-weight: bold; text-decoration: none;">CDClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB) 0.1(6H, s, <del style="font-weight: bold; text-decoration: none;">2CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB on Si), 0.9(9H, s, <del style="font-weight: bold; text-decoration: none;">3CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB on tert-butyl), 1.55-1.7(15H, m, <del style="font-weight: bold; text-decoration: none;">5CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB on geranylgeranyl), 1.95-3.15(12H, br m, <del style="font-weight: bold; text-decoration: none;">6CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">12</del>/FONT/SUB on geranylgeranyl), 3.45-3.70(5H, br m), 4.18[2H, d, J=6.7Hz H at C(1) on geranylgeranyl], 4.58(2H, s, <del style="font-weight: bold; text-decoration: none;">CHSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">12</del>/FONT/SUB), 5.0-5.2[3H m, H at C(6), C(10) and C(14)], 5.4 [1H, t, J=6.7Hz H at C(2) on geranylgeranyl], 7.25(5H, br m)<del style="font-weight: bold; text-decoration: none;">BRSUPFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">11</del>/FONT/<del style="font-weight: bold; text-decoration: none;">SUPSUPFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/<del style="font-weight: bold; text-decoration: none;">SUPC </del>NMR(75MHz, <del style="font-weight: bold; text-decoration: none;">CDClSUBFONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">13</del>/FONT/SUB)-5,2(q), 16.0(q), 16.5(q), 17.7(q), 18.2(q), 18.5(s), 25.2(q), 25.9(q), 26.37(t), 26.44(t), 27.8(t), 39.6(t), 39.7(t), 63.0(t), 66.9(t), 70.2(t), 73.5(t), 78.5(d), 121.2(d), 123.9(d), 124.2(d), 124.4(d), 127.46(d), 127.50(d), 128.3(d), 128.5(s), 132.0(s), 134.9(s), 135.2(s), 139.7(s)0174, </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=<ins style="font-weight: bold; text-decoration: none;"><SUP><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>1<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/<ins style="font-weight: bold; text-decoration: none;">SUP>H </ins>NMR (300MHz,<ins style="font-weight: bold; text-decoration: none;">CDCl<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>3<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">></ins>) 0.1(6H, s, <ins style="font-weight: bold; text-decoration: none;">2CH<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>3<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">> </ins>on Si), 0.9(9H, s, <ins style="font-weight: bold; text-decoration: none;">3CH<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>3<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">> </ins>on tert-butyl), 1.55-1.7(15H, m, <ins style="font-weight: bold; text-decoration: none;">5CH<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>3<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">> </ins>on geranylgeranyl), 1.95-3.15(12H, br m, <ins style="font-weight: bold; text-decoration: none;">6CH<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>2<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">> </ins>on geranylgeranyl), 3.45-3.70(5H, br m), 4.18[2H, d, J=6.7Hz H at C(1) on geranylgeranyl], 4.58(2H, s, <ins style="font-weight: bold; text-decoration: none;">CH<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>2<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">></ins>), 5.0-5.2[3H m, H at C(6), C(10) and C(14)], 5.4 [1H, t, J=6.7Hz H at C(2) on geranylgeranyl], 7.25(5H, br m)<ins style="font-weight: bold; text-decoration: none;"><BR><SUP><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>1<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/<ins style="font-weight: bold; text-decoration: none;">SUP><SUP><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>3<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/<ins style="font-weight: bold; text-decoration: none;">SUP>C </ins>NMR(75MHz, <ins style="font-weight: bold; text-decoration: none;">CDCl<SUB><FONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">1>3<</ins>/FONT<ins style="font-weight: bold; text-decoration: none;">><</ins>/SUB<ins style="font-weight: bold; text-decoration: none;">></ins>)-5,2(q), 16.0(q), 16.5(q), 17.7(q), 18.2(q), 18.5(s), 25.2(q), 25.9(q), 26.37(t), 26.44(t), 27.8(t), 39.6(t), 39.7(t), 63.0(t), 66.9(t), 70.2(t), 73.5(t), 78.5(d), 121.2(d), 123.9(d), 124.2(d), 124.4(d), 127.46(d), 127.50(d), 128.3(d), 128.5(s), 132.0(s), 134.9(s), 135.2(s), 139.7(s)<ins style="font-weight: bold; text-decoration: none;"><<</ins>0174<ins style="font-weight: bold; text-decoration: none;">>></ins>, </div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Chromatograms=chromatography on silica (Rf=0.57, ethyl acetate-hexane(2:23) )0174, </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Chromatograms=chromatography on silica (Rf=0.57, ethyl acetate-hexane(2:23) )<ins style="font-weight: bold; text-decoration: none;"><<</ins>0174<ins style="font-weight: bold; text-decoration: none;">>></ins>, </div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>}}</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><br></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Lipid/Footer}}</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Lipid/Footer}}</div></td></tr>
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">← Older revision</td>
<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 05:00, 28 January 2010</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=EEL0209</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=EEL0209</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Common Name=<del style="font-weight: bold; text-decoration: none;">&& </del>(S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol<del style="font-weight: bold; text-decoration: none;">&&</del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Common Name= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[<del style="font-weight: bold; text-decoration: none;"><</del>FONT FACE=<del style="font-weight: bold; text-decoration: none;">"Symbol">a<</del>/FONT<del style="font-weight: bold; text-decoration: none;">></del>]<del style="font-weight: bold; text-decoration: none;"><sub>D<</del>/<del style="font-weight: bold; text-decoration: none;">sub><sup>25<</del>/sup<del style="font-weight: bold; text-decoration: none;">></del>=-2.4° (C3.2, <del style="font-weight: bold; text-decoration: none;">CHCl<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>3<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">></del>)<del style="font-weight: bold; text-decoration: none;"><<</del>0174<del style="font-weight: bold; text-decoration: none;">>></del></div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[FONT FACE=<ins style="font-weight: bold; text-decoration: none;">Symbola</ins>/FONT]<ins style="font-weight: bold; text-decoration: none;">subD</ins>/<ins style="font-weight: bold; text-decoration: none;">subsup25</ins>/sup=-2.4° (C3.2, <ins style="font-weight: bold; text-decoration: none;">CHClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB)0174</div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<del style="font-weight: bold; text-decoration: none;"><<</del>0174<del style="font-weight: bold; text-decoration: none;">>></del>, </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)0174, </div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=<del style="font-weight: bold; text-decoration: none;"><SUP><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>1<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/<del style="font-weight: bold; text-decoration: none;">SUP>H </del>NMR (300MHz,<del style="font-weight: bold; text-decoration: none;">CDCl<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>3<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">></del>) 0.1(6H, s, <del style="font-weight: bold; text-decoration: none;">2CH<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>3<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">> </del>on Si), 0.9(9H, s, <del style="font-weight: bold; text-decoration: none;">3CH<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>3<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">> </del>on tert-butyl), 1.55-1.7(15H, m, <del style="font-weight: bold; text-decoration: none;">5CH<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>3<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">> </del>on geranylgeranyl), 1.95-3.15(12H, br m, <del style="font-weight: bold; text-decoration: none;">6CH<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>2<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">> </del>on geranylgeranyl), 3.45-3.70(5H, br m), 4.18[2H, d, J=6.7Hz H at C(1) on geranylgeranyl], 4.58(2H, s, <del style="font-weight: bold; text-decoration: none;">CH<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>2<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">></del>), 5.0-5.2[3H m, H at C(6), C(10) and C(14)], 5.4 [1H, t, J=6.7Hz H at C(2) on geranylgeranyl], 7.25(5H, br m)<del style="font-weight: bold; text-decoration: none;"><BR><SUP><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>1<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/<del style="font-weight: bold; text-decoration: none;">SUP><SUP><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>3<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/<del style="font-weight: bold; text-decoration: none;">SUP>C </del>NMR(75MHz, <del style="font-weight: bold; text-decoration: none;">CDCl<SUB><FONT </del>SIZE=-<del style="font-weight: bold; text-decoration: none;">1>3<</del>/FONT<del style="font-weight: bold; text-decoration: none;">><</del>/SUB<del style="font-weight: bold; text-decoration: none;">></del>)-5,2(q), 16.0(q), 16.5(q), 17.7(q), 18.2(q), 18.5(s), 25.2(q), 25.9(q), 26.37(t), 26.44(t), 27.8(t), 39.6(t), 39.7(t), 63.0(t), 66.9(t), 70.2(t), 73.5(t), 78.5(d), 121.2(d), 123.9(d), 124.2(d), 124.4(d), 127.46(d), 127.50(d), 128.3(d), 128.5(s), 132.0(s), 134.9(s), 135.2(s), 139.7(s)<del style="font-weight: bold; text-decoration: none;"><<</del>0174<del style="font-weight: bold; text-decoration: none;">>></del>, </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|NMR Spectra=<ins style="font-weight: bold; text-decoration: none;">SUPFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">11</ins>/FONT/<ins style="font-weight: bold; text-decoration: none;">SUPH </ins>NMR (300MHz,<ins style="font-weight: bold; text-decoration: none;">CDClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB) 0.1(6H, s, <ins style="font-weight: bold; text-decoration: none;">2CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB on Si), 0.9(9H, s, <ins style="font-weight: bold; text-decoration: none;">3CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB on tert-butyl), 1.55-1.7(15H, m, <ins style="font-weight: bold; text-decoration: none;">5CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB on geranylgeranyl), 1.95-3.15(12H, br m, <ins style="font-weight: bold; text-decoration: none;">6CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">12</ins>/FONT/SUB on geranylgeranyl), 3.45-3.70(5H, br m), 4.18[2H, d, J=6.7Hz H at C(1) on geranylgeranyl], 4.58(2H, s, <ins style="font-weight: bold; text-decoration: none;">CHSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">12</ins>/FONT/SUB), 5.0-5.2[3H m, H at C(6), C(10) and C(14)], 5.4 [1H, t, J=6.7Hz H at C(2) on geranylgeranyl], 7.25(5H, br m)<ins style="font-weight: bold; text-decoration: none;">BRSUPFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">11</ins>/FONT/<ins style="font-weight: bold; text-decoration: none;">SUPSUPFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/<ins style="font-weight: bold; text-decoration: none;">SUPC </ins>NMR(75MHz, <ins style="font-weight: bold; text-decoration: none;">CDClSUBFONT </ins>SIZE=-<ins style="font-weight: bold; text-decoration: none;">13</ins>/FONT/SUB)-5,2(q), 16.0(q), 16.5(q), 17.7(q), 18.2(q), 18.5(s), 25.2(q), 25.9(q), 26.37(t), 26.44(t), 27.8(t), 39.6(t), 39.7(t), 63.0(t), 66.9(t), 70.2(t), 73.5(t), 78.5(d), 121.2(d), 123.9(d), 124.2(d), 124.4(d), 127.46(d), 127.50(d), 128.3(d), 128.5(s), 132.0(s), 134.9(s), 135.2(s), 139.7(s)0174, </div></td></tr>
<tr><td class="diff-marker" data-marker="−"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #ffe49c; vertical-align: top; white-space: pre-wrap;"><div>|Chromatograms=chromatography on silica (Rf=0.57, ethyl acetate-hexane(2:23) )<del style="font-weight: bold; text-decoration: none;"><<</del>0174<del style="font-weight: bold; text-decoration: none;">>></del>, </div></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div>|Chromatograms=chromatography on silica (Rf=0.57, ethyl acetate-hexane(2:23) )0174, </div></td></tr>
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<p><a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013:01" class="mw-redirect" title="LBG00ukk:R:16402BC01:CBZ1Sk013:01">LBG00ukk:R:16402BC01:CBZ1Sk013:01</a> moved to <a href="/wiki/LBG00ukk:R:16402BC01:CBZ1Sk013" title="LBG00ukk:R:16402BC01:CBZ1Sk013">LBG00ukk:R:16402BC01:CBZ1Sk013</a></p>
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2009-07-26T13:00:00Z
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 22:00, 26 July 2009</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Metabolite</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>{{Metabolite</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=EEL0209</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=EEL0209</div></td></tr>
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Editor at 12:00, 8 July 2009
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 21:00, 8 July 2009</td>
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Editor at 11:00, 8 July 2009
2009-07-08T11:00:00Z
<p></p>
<table style="background-color: #fff; color: #202122;" data-mw="interface">
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<td colspan="2" style="background-color: #fff; color: #202122; text-align: center;">Revision as of 20:00, 8 July 2009</td>
</tr><tr><td colspan="2" class="diff-lineno" id="mw-diff-left-l2">Line 2:</td>
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<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=EEL0209</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|LipidBank=EEL0209</div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|SysName= (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol</div></td></tr>
<tr><td colspan="2" class="diff-side-deleted"></td><td class="diff-marker" data-marker="+"></td><td style="color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #a3d3ff; vertical-align: top; white-space: pre-wrap;"><div><ins style="font-weight: bold; text-decoration: none;">|Common Name=&& (S) -1-O- (tert-butyldimethylsilyl) -2-O-geranylgeranyl-3-O-benzylglycerol&&</ins></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>25</sup>=-2.4° (C3.2, CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>)<<0174>></div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Reflactive=[<FONT FACE="Symbol">a</FONT>]<sub>D</sub><sup>25</sup>=-2.4° (C3.2, CHCl<SUB><FONT SIZE=-1>3</FONT></SUB>)<<0174>></div></td></tr>
<tr><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<<0174>>, </div></td><td class="diff-marker"></td><td style="background-color: #f8f9fa; color: #202122; font-size: 88%; border-style: solid; border-width: 1px 1px 1px 4px; border-radius: 0.33em; border-color: #eaecf0; vertical-align: top; white-space: pre-wrap;"><div>|Mass Spectra=(CI methane) 69(61.9), 81(40.9), 91(90.9), 109(15.5), 121(15.1), 137(18.9), 149(15.7), 163(7.4), 175(3.3), 189(8.6), 217(9.1), 239(11.4), 257(2.2), 273(19.4), 297(100), 568(M+1, 2.0)<<0174>>, </div></td></tr>
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