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(3R,5S)-5-[[N-(3-AMINOPROPYL)-CARBAMOYL]-OXY]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE

Compound with spectra: 2 NMR

(3R,5S)-5-[[N-(3-AMINOPROPYL)-CARBAMOYL]-OXY]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
SpectraBase Compound ID 1LnNPofpart
InChI InChI=1S/C13H20N2O3/c1-3-10-7-11(8-12(16)9(10)2)18-13(17)15-6-4-5-14/h1,11-12,16H,4-8,14H2,2H3,(H,15,17)/t11-,12+/m0/s1
InChIKey YLECRYSPWXOPTC-NWDGAFQWSA-N
Mol Weight 252.31 g/mol
Molecular Formula C13H20N2O3
Exact Mass 252.147393 g/mol
Enantiomer InChIKey YLECRYSPWXOPTC-NEPJUHHUSA-N

View Spectrum of (3R,5S)-5-[[N-(3-AMINOPROPYL)-CARBAMOYL]-OXY]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of (3R,5S)-5-[[N-(3-AMINOPROPYL)-CARBAMOYL]-OXY]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
  • (3S,5R)-5-([N-(3-AMINOPROPYL)-CARBAMOYL]-OXY)-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
(3R,5S)/(3R,5R)-5-[[N-(3-AMINOPROPYL)-CARBAMOYL]-OXY]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
(3S,5R)-5-([N-BUTYLCARBAMOYL]-OXY)-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
(3S,5R)-1-ETHYNYL-3-HYDROXY-5-([N-(6-HYDROXYHEXYL)-CARBAMOYL]-OXY)-2-METHYL-1-CYCLOHEXENE
(3S,5R)-1-ETHYNYL-3-HYDROXY-5-([N-(2-HYDROXYETHYL)-CARBAMOYL]-OXY)-2-METHYL-1-CYCLOHEXENE
(3S,5S)/(3R,5R)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE
(3R,5S)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE
(R)-4-Ethynyl-3,5,5-trimethylcyclohex-3-enyl Acetate
2-[(1S,3S,5R)-5-acetoxy-3-hydroxy-2-methylene-cyclohexyl]acetic acid methyl ester
3,5-Dihydroxy-4,6-dimethylnonan-7-yl phenylcarbamate
Bicyclo[3.2.1]oct-6-ene, 2,8-dimethoxy-
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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