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#46;[3R,6R,7S,(8E),10S,11S,(12E)]-7-(ACETYLOXY)-3-[[TERT.-BUTYL-(DIMETHYL)-SILYL]-OXY]-11-HYDROXY-13-IODO-6-[(2-METHOXYETHOXY)-METHOXY]-6,10,12-TRIMETHYL-TRIDE

Compound with spectra: 1 NMR

#46;[3R,6R,7S,(8E),10S,11S,(12E)]-7-(ACETYLOXY)-3-[[TERT.-BUTYL-(DIMETHYL)-SILYL]-OXY]-11-HYDROXY-13-IODO-6-[(2-METHOXYETHOXY)-METHOXY]-6,10,12-TRIMETHYL-TRIDE
SpectraBase Compound ID JbCdTMIXc3G
InChI InChI=1S/C28H51IO9Si/c1-20(26(33)21(2)18-29)11-12-24(37-22(3)30)28(7,36-19-35-16-15-34-8)14-13-23(17-25(31)32)38-39(9,10)27(4,5)6/h11-12,18,20,23-24,26,33H,13-17,19H2,1-10H3,(H,31,32)/b12-11+,21-18+/t20-,23+,24-,26-,28+/m0/s1
InChIKey OEFCPNGKSBWWGU-JXKBNNTPSA-N
Mol Weight 686.7 g/mol
Molecular Formula C28H51IO9Si
Exact Mass 686.234705 g/mol
Enantiomer InChIKey OEFCPNGKSBWWGU-FDNFCTBCSA-N

View Spectrum of #46;[3R,6R,7S,(8E),10S,11S,(12E)]-7-(ACETYLOXY)-3-[[TERT.-BUTYL-(DIMETHYL)-SILYL]-OXY]-11-HYDROXY-13-IODO-6-[(2-METHOXYETHOXY)-METHOXY]-6,10,12-TRIMETHYL-TRIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
GIBBEROSENE_D;(4-S*,11-S*,12-R*,13-S*,2-E,7-E,14-Z)-13-ACETOXY-11,12-ACETOXY-11,12-EPOXY-4-HYDROXYCEMBRA-2,7,14-TRIENE
UPUJAIKAYWQYDO-QRFHUDMDSA-N
(1S,2S,3S,4S,6R,7S)-1,4-DI-O-TERT.-BUTYLDIMETHYLSILYL-2,3-O-METHYLETHYLIDENE-CYCLOOCTANE-1,2,3,4,6,7-HEXOL
(1R,2S,3S,4R,6R,7S)-1,4-DI-O-TERT.-BUTYLDIMETHYLSILYL-2,3-O-METHYLETHYLIDENE-CYCLOOCTANE-1,2,3,4,6,7-HEXOL
(1R,3R,4S,5R)-1,4-Dihydroxy-3-[(tert-butyldimethylsilyl)oxy]-6-oxa-bicyclo[3.2.1]octan-7-one
(3S,6R,7S,8S)-3,7-bis[[tert-butyl(dimethyl)silyl]oxy]-4,4,6,8-tetramethyl-5-oxidanylidene-tridec-12-enoic acid
ZAWADSKINOLIDE-E;15-ACETOXY-1-BETA,3-BETA-DIHYDROXY-GERMACRA-4Z,10(14)-DIEN-6-BETA,7-ALPHA,11-ALPHA-12,6-OLIDE
(7R)-2,8(19),12(20)-6,7,11-tris(Acetoxy)cembratiene-4-ol
QHSHRGAPMNYBQO-DIJBOSQOSA-N
SINUFLEXIBILIN-B
Title Journal or Book Year
Synthesis of Pladienolide B and Its 7-Epimer with Insights into the Role of the Allylic Acetate European Journal of Organic Chemistry 2013
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