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(1R,4S,5R,7S)-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-7-CHLORO-3-HYDROXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER

Compound with spectra: 1 NMR

(1R,4S,5R,7S)-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-7-CHLORO-3-HYDROXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER
SpectraBase Compound ID Bvu1fOv9EwI
InChI InChI=1S/C18H31ClO4Si/c1-16(2,3)24(7,8)23-18(5)11-9-12(17(4,19)10-11)13(14(18)20)15(21)22-6/h11-12,20H,9-10H2,1-8H3/t11-,12-,17+,18+/m1/s1
InChIKey ABDVVXFBRYMANG-VVDPLQPHSA-N
Mol Weight 374.98 g/mol
Molecular Formula C18H31ClO4Si
Exact Mass 374.168014 g/mol
Enantiomer InChIKey ABDVVXFBRYMANG-YDOWWZDFSA-N

View Spectrum of (1R,4S,5R,7S)-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-7-CHLORO-3-HYDROXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1R,4S,5R,7S)-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-3,7-DIHYDROXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER
(1R,4S,5R,7S)-4-(TERT.-BUTYLDIMETHYLSILANYLOXY)-3-HYDROXY-7-METHOXY-4,7-DIMETHYL-BICYCLO-[3.2.1]-OCT-2-ENE-2-CARBOXILIC-ACID-METHYLESTER
GARCINIAPHENONE;(1R,5S,7S)-3-BENZOYL-4-HYDROXY-6,6-DIMETHYL-5,7-DI-(3-METHYL-2-BUTENYL)-BICYCLO-[3.3.1]-NON-3-ENE-2,9-DIONE
Androsta-2,4,6-triene-2-carboxaldehyde, 3-chloro-17.beta.-hydroxy-, acetate
Coumachlor-A (-H2O)
1-ALPHA,4-ALPHA-DIHYDROXY-9-ALPHA-ACETOXY-GUAIA-10(14),2-DIENE-12,6-ALPHA-OLIDE
Sipholenol-E,monoacetate
HUMIFUSIN-B
(3aS*,6S*,6aS*,9S*,9aS*,9bS*)-3a,4,5,6,6a,9,9a,9b-Octahydro-6,6a,9-trihydroxy-6,9-dimethyl-3-methyleneazuleno[4,5-b]furan-2(3H)-one
DIHYDROPRENYL-5,6,7,8-TETRAHYDRO-LAPACHOYL-17-BETA-DIHYDRO-JUNICEDRATE-METHYLESTER
Title Journal or Book Year
Synthesis of Highly Functionalised Enantiopure Bicyclo[3.2.1]- octane Systems from Carvone Molecules 2004
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