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

Compound with spectra: 1 NMR

(1R,3AR,4R,5R,6AS)-1,4-DIALLYL-5-[[TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-HEXAHYDROPENTALEN-2(1H)-ONE
SpectraBase Compound ID 8gLbafwuqIi
InChI InChI=1S/2C20H34O2Si/c1-8-10-15-17(21)12-14-13-18(16(11-9-2)19(14)15)22-23(6,7)20(3,4)5;1-8-10-14-17-13-19(22-23(6,7)20(3,4)5)15(11-9-2)16(17)12-18(14)21/h8-9,14-16,18-19H,1-2,10-13H2,3-7H3;8-9,14-17,19H,1-2,10-13H2,3-7H3/t14-,15+,16-,18-,19+;14-,15-,16-,17-,19+/m01/s1
InChIKey JVPYXVJQWHQGIB-ZWDBQMBNSA-N
Mol Weight 669.2 g/mol
Molecular Formula C40H68O4Si2
Exact Mass 668.465614 g/mol
Enantiomer InChIKey JVPYXVJQWHQGIB-WWZLYCRISA-N

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

13C NMR Spectrum
Copyright Copyright © 2016-2025 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#18A;N'-[(1R,(2E),3AS,4R,5R,6AS)-4-ALLYL-5-[[TERT.-BUTYL-(DIPHENYL)-SILYL]-OXY]-1-METHYLHEXAHYDROPENTALEN-2(1H)-YLIDENE]-4-METHYLBENZENESULFONOHYDRAZIDE
1-A-H,5-A-H-GUAIA-10(14),11(13)-DIEN-12,6-A-OLIDE,15-ETHOXY-3-OXO
2-Phenyl-3-ethoxycarbonyl-4,7-methano-octahydroinden-1-one
(1S,4S,5R)-4-[(1S)-1-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-HYDROXYETHYL]-7,7-DIMETHYL-1-VINYL-2-OXABICYCLO-[3.2.0]-HEPTAN-3-ONE
(1S,4R,5S)-4-[(1S)-1-(TERT.-BUTYLDIMETHYLSILYLOXY)-2-HYDROXYETHYL]-7,7-DIMETHYL-1-VINYL-2-OXABICYCLO-[3.2.0]-HEPTAN-3-ONE
tert-Butyl-dimethyl-[(1R,2R,6S)-6,9,9-trimethylspiro[bicyclo[4.2.1]nonane-8,2'-oxirane]-2-yl]oxy-silane
(1R*,4S*,5S*,7S*,9S*,10R*)-10-TERT.-BUTOXY-5-TERT.-BUTYLDIMETHYLSILOXY-4,7-DIMETHYL-2-OXO-BICYCLO-[5.3.0]-DECANE-9-CARBALDEHYDE
(2S,3S,4aS,5S,8aR)-3-[tert-butyl(dimethyl)silyl]oxy-2-methyl-5-[(1E,3E)-octa-1,3-dienyl]-3,4,4a,5,6,7,8,8a-octahydro-2H-quinoline-1-carboxylic acid tert-butyl ester
(1R,4S,4aR,9aS)-1,2,3,4,4a,9a-hexahydro-8-methoxy-1,4-methanofluoren-9-one
3-(tert-Butyl)-4-(4-fluorobenzoyl)-1-methyl-1,4,5,7-tetrahydro-6H-pyrazolo[3,4-b]pyridin-6-one
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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