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(1S*,3R*,7R*,9S*,10S*,12R*,14R*)-12-ACETOXYALLYLMETHYL-10-HYDROXY-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE

Compound with spectra: 1 NMR

(1S*,3R*,7R*,9S*,10S*,12R*,14R*)-12-ACETOXYALLYLMETHYL-10-HYDROXY-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE
SpectraBase Compound ID H2EazpPGIGG
InChI InChI=1S/C24H40O6/c1-5-6-7-9-18-10-8-11-24(4)22(29-18)14-21-23(30-24)20(26)13-19(28-21)12-16(2)15-27-17(3)25/h18-23,26H,2,5-15H2,1,3-4H3/t18-,19-,20+,21-,22+,23+,24-/m1/s1
InChIKey XGZCDSWIYGSFSD-USUYLUBRSA-N
Mol Weight 424.6 g/mol
Molecular Formula C24H40O6
Exact Mass 424.282489 g/mol
Enantiomer InChIKey XGZCDSWIYGSFSD-XJDLZNRKSA-N

View Spectrum of (1S*,3R*,7R*,9S*,10S*,12R*,14R*)-12-ACETOXYALLYLMETHYL-10-HYDROXY-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1S*,3R*,7R*,9S*,10S*,12R*,14R*)-10-HYDROXY-12-HYDROXYALLYLMETHYL-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE
(1S*,3R*,7R*,9S*,10S*,12R*,14R*)-10-HYDROXY-12-(2'-FORMYL)-ALLYL-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE
(1S*,3R*,7R*,9S*,10S*,12R*/12S*14R*)-10-HYDROXY-12-METHOXY-7-METHYL-3-PENTYL-2,8,13-TRIOXATRICYCLO-[8.5.0.0(9,14)]-PENTADECANE;MAJOR-ISOMER
METHYL-(2,3,4,6-TETRA-O-METHYL-BETA-D-MANNOPYRANOSYL)-(1->4A)-2,3-DI-O-METHYL-4A-CARBA-ALPHA-D-GLUCOPYRANOSIDE
2,3,4,6-Tetra-o-methyl-.beta.-D-glucopyranosyl 4,6-di-o-methyl-1,2,5-tri-o-TMS-D-galactitol
TRIACETYLCYCLOCLINACOSIDE-A2
1,2-BIS-[[(2,3,4,6-TETRA-O-ACETYL-ALPHA-D-MANNOPYRANOSYLOXY)-METHYL]-1H-1,2,3-TRIAZOLETHOXY]-ETHANE
D-Galactose, O-2,3,4,6-tetra-O-methyl-.beta.-D-glucopyranosyl-(1.fwdarw.2)-O-3,4,6-tri-O-methyl-.beta.-D-glucopyranosyl-(1.fwdarw.4)-2,3,5,6-tetra-O-methyl-
E-1,3,4,6-Tetra-O-acetyl-2-deoxy-2-formamide-A-D -glucopyranose
DENDRONPHOLIDE_K
Title Journal or Book Year
Development of an Approach to the Synthesis of the ABC Ring System of Hemibrevetoxin B Organic Letters 2006
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