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(1R,3AR,4R,5R,6AS)-4-ALLYL-5-[[TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-1-METHYLHEXAHYDROPENTALEN-2(1H)-ONE

Compound with spectra: 1 NMR

(1R,3AR,4R,5R,6AS)-4-ALLYL-5-[[TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-1-METHYLHEXAHYDROPENTALEN-2(1H)-ONE
SpectraBase Compound ID Ewu8HWtjUJq
InChI InChI=1S/C18H32O2Si/c1-8-9-13-15-10-16(19)12(2)14(15)11-17(13)20-21(6,7)18(3,4)5/h8,12-15,17H,1,9-11H2,2-7H3/t12-,13-,14-,15-,17-/m1/s1
InChIKey GVHZNBUJVGOYJB-DRXUAVOGSA-N
Mol Weight 308.5 g/mol
Molecular Formula C18H32O2Si
Exact Mass 308.217157 g/mol
Enantiomer InChIKey GVHZNBUJVGOYJB-BWJWTDLKSA-N

View Spectrum of (1R,3AR,4R,5R,6AS)-4-ALLYL-5-[[TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-1-METHYLHEXAHYDROPENTALEN-2(1H)-ONE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(Z)-2-((3aS,4S,5R,6aS)-5-((tert-butyldimethylsilyl)oxy-4-(tert-butyldimethylsilyl)oxy)methyl)hexahydropentalen-2(1H)-ylidene)ethanol
(E)-2-((3aS,4S,5R,6aS)-5-((tert-Butyldimethylsilyl)oxy-4-(tert-butyldimethylsilyl)oxy)methyl)hexahydropentalen-2(1H)-ylidene)ethanol
N'-[(1R,(2E),3AS,4R,5R,6AS)-4-ALLYL-5-HYDROXY-1-METHYLHEXAHYDROPENTALEN-2(1H)-YLIDENE]-4-METHYLBENZENESULFONOHYDRAZIDE
(3AS,4R,5R,6AR)-5-[[TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-4-METHYLHEXAHYDROPENTALEN-2(1H)-ONE
(1S,2S,3R,4S)-4-(tert-Butyldimethylsilanyloxy)-3-(tert-butyldimethylsilanyloxymethyl)-2-chloromethylcyclopentanecarboxylic acid acid methyl ester
(.alpha.S,exo,exo)-.alpha.-Methyl-6-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]bicyclo[2.2.1]heptane-2-methanol .alpha.-(4-Methylbenzenesulfonate
(.alpha.R,exo,exo)-.alpha.-Methyl-6-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]bicyclo[2.2.1]heptane-2-methanol .alpha.-(4-Methylbenzenesulfonate
Methyl (1S*,2S*,4aR*,8S*,8aS*)-8-(tert-butyldimethylsiloxy)-2-methyl-1,2,4a,5,6,7,8,8a-octahydronaphthalenepropanoate
CYCLOPENTA[C]PYRAN-3(1H)-ONE, 6-(ACETYLOXY)-7-[(ACETYLOXY)METHYL]HEXAHYDRO-4-METHYL-
Methyl (13E)-6-oxo-9,11,15-tris[(trimethylsilyl)oxy]prost-13-en-1-oate
Title Journal or Book Year
Doing it Twice: Asymmetric Deprotonation/Alkylation of Weiss Diketone Derivatives as Key Steps in the Functionalization of Bicyclo[3.3.0]octanes European Journal of Organic Chemistry 2012
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