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(3R,5S)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE

Compound with spectra: 2 NMR

(3R,5S)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE
SpectraBase Compound ID KDRouBcuRI6
InChI InChI=1S/C12H14O4/c1-4-9-6-10(7-11(13)8(9)3)16-12(14)15-5-2/h1,5,10-11,13H,2,6-7H2,3H3/t10-,11+/m0/s1
InChIKey LTFUMIMQLZYRTB-WDEREUQCSA-N
Mol Weight 222.24 g/mol
Molecular Formula C12H14O4
Exact Mass 222.089209 g/mol
Enantiomer InChIKey LTFUMIMQLZYRTB-MNOVXSKESA-N

View Spectrum of (3R,5S)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (3R,5S)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (3S,5R)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(VINYLOXY)-CARBONYL]-1-CYCLOHEXENE
(3S,5S)/(3R,5R)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE
(3S,5R)-1-ETHYNYL-3-HYDROXY-5-(METHOXYCARBONYL)-2-METHYL-1-CYCLOHEXENE
(3R,5S)-5-(CARBAZOYLOXY)-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
(3S,5S)/(3R,5R)-5-(CARBAZOYLOXY)-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
(3R,5S)-5-[[N-(3-AMINOPROPYL)-CARBAMOYL]-OXY]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
cis-Methyl 2,3-Dimethyl-5-methoxy-2-cyclohexene-1-carboxylate
trans-Methyl 2,3-Dimethyl-5-methoxy-2-cyclohexene-1-carboxylate
MESO-(1R,1'S,6R,6'S)-3,3'-METHYLENEBIS-[6-[(BENZYLOXY)-METHOXY]-CYCLOHEPT-3-EN-1-OL
MIRABILENE-A-FORMAMIDE
VCVGYWAHYNJRQC-NPIHAVRMSA-N
Title Journal or Book Year
1α,25-Dihydroxyvitamin D3 A-Ring Precursors:  Studies on Regioselective Enzymatic Alkoxycarbonylation Reactions of Their Stereoisomers. Chemoenzymatic Synthesis of A-Ring Synthon Carbamate Derivatives, Including Carbazates and Polyamino Carbamates The Journal of Organic Chemistry 1999
Selective Alkoxycarbonylation of A-Ring Precursors of Vitamin D Using Enzymes in Organic Solvents. Chemoenzymatic Synthesis of 1α,25-Dihydroxyvitamin D3 C-5 A-Ring Carbamate Derivatives1 The Journal of Organic Chemistry 1997
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