(3S,5R)-1-ETHYNYL-3-HYDROXY-2-METHYL-5-(PHENOXYCARBONYL)-1-CYCLOHEXENE
Compound with spectra: 1 NMR
| SpectraBase Compound ID | LReS5rspxNm |
|---|---|
| InChI | InChI=1S/C16H16O4/c1-3-12-9-14(10-15(17)11(12)2)20-16(18)19-13-7-5-4-6-8-13/h1,4-8,14-15,17H,9-10H2,2H3/t14-,15+/m0/s1 |
| InChIKey | ZPNAKKYQLYYDPJ-LSDHHAIUSA-N |
| Mol Weight | 272.3 g/mol |
| Molecular Formula | C16H16O4 |
| Exact Mass | 272.104859 g/mol |
| Enantiomer InChIKey | ZPNAKKYQLYYDPJ-CABCVRRESA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
(3S,5S)/(3R,5R)-1-Ethynyl-3-hydroxy-2-methyl-5-[(acetonoxime)carbonyloxy]cyclohex-1-ene
(3R,5R)-1-ETHYNYL-5-HYDROXY-2-METHYL-3-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE
(3R,5S)-1-ETHYNYL-5-HYDROXY-2-METHYL-3-[(VINYLOXY)-CARBONYLOXY]-1-CYCLOHEXENE
[(1R,5R)-3-ethynyl-5-hydroxy-2-methyl-1-cyclohex-2-enyl] (propan-2-ylideneamino) carbonate
(3S,5R)-3-[(TERT.-BUTOXYCARBONYL)-AMINO]-1-ETHYNYL-5-HYDROXY-2-METHYLCYCLOHEX-1-ENE
(E,6S,7S)-8-[tert-butyl(dimethyl)silyl]oxy-2,6-dimethyl-7-phenoxycarbothioyloxy-oct-2-enoic acid methyl ester
Ethyl (2Z,6S,7S)-8-tert-Butyldimethylsiloxy-2,6-dimethyl-7-[(phenoxythiocarbonyl)oxy]-2-octenoate
(E,6S,7S)-8-[tert-butyl(dimethyl)silyl]oxy-2,6-dimethyl-7-phenoxycarbothioyloxy-oct-2-enoic acid ethyl ester
(S)-3-Ethynyl-2,4,4-trimethylcyclohex-2-en-1-yl - Acetate
6R-(4'R,6'R-ACETONIDE-8'-PHENYLOCT-1'-ENYL)-5,6-DIHYDRO-2H-PYRAN-2-ONE;STRICTIFOLIONE-4'R,6'R-ACETONIDE
| Title | Journal or Book | Year |
|---|---|---|
| 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 |
This compound is available in the following databases:
KnowItAll NMR Spectral Library
Author: Wiley
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