John Wiley & Sons, Inc. SpectraBase; SpectraBase Compound ID=17idDwF7BON

(accessed ).
(3R,5S)-5-(CARBAMOYLOXY)-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
SpectraBase Compound ID 17idDwF7BON
InChI InChI=1S/C10H13NO3/c1-3-7-4-8(14-10(11)13)5-9(12)6(7)2/h1,8-9,12H,4-5H2,2H3,(H2,11,13)/t8-,9+/m0/s1
InChIKey CBZBUUCBFVFNPN-DTWKUNHWSA-N
Mol Weight 195.22 g/mol
Molecular Formula C10H13NO3
Exact Mass 195.089543 g/mol
Enantiomer InChIKey CBZBUUCBFVFNPN-BDAKNGLRSA-N
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
Copyright Copyright © 2016-2020 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD
  • (3S,5R)-5-(CARBAMOYLOXY)-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
Title Journal or Book Year
1α,25-Dihydroxyvitamin D3A-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 D3C-5 A-Ring Carbamate Derivatives1 The Journal of Organic Chemistry 1997
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