(3S,5R)-5-[(BENZYLOXY)-CARBONYL]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE
Compound with spectra: 1 NMR
![(3S,5R)-5-[(BENZYLOXY)-CARBONYL]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE](/api/compound/AHJj4FGqYMU.png?ph=true&h=300&w=458 "(3S,5R)-5-[(BENZYLOXY)-CARBONYL]-1-ETHYNYL-3-HYDROXY-2-METHYL-1-CYCLOHEXENE")
| SpectraBase Compound ID | AHJj4FGqYMU |
|---|---|
| InChI | InChI=1S/C17H18O4/c1-3-14-9-15(10-16(18)12(14)2)21-17(19)20-11-13-7-5-4-6-8-13/h1,4-8,15-16,18H,9-11H2,2H3/t15-,16+/m0/s1 |
| InChIKey | DJTVFMBNDLXVJQ-JKSUJKDBSA-N |
| Mol Weight | 286.33 g/mol |
| Molecular Formula | C17H18O4 |
| Exact Mass | 286.120509 g/mol |
| Enantiomer InChIKey | DJTVFMBNDLXVJQ-CVEARBPZSA-N |
| 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-(PHENOXYCARBONYL)-1-CYCLOHEXENE
(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
Benzyl 8-(5-methoxy-3,6-dioxo-cyclohexa-1,4-dienyl)-octyl carbonate
(3S,5R)-3-[(TERT.-BUTOXYCARBONYL)-AMINO]-1-ETHYNYL-5-HYDROXY-2-METHYLCYCLOHEX-1-ENE
(1S*,4S*,6R*)-4-(3-Benzyloxy-propyl)-5-isopropylidene-3-oxabicyclo[4.1.0]heptane
(3S,4S,2'R,1''Z)-3-(1''-HEXENYL)-4-(2'-PHENYLMETHYLOXY-TRIDECYL)-2-OXETANONE
#29;(-)-(3S)-4-[(4R,6R)-6-[[(4R,6S)-6-[(2R,4S)-4-HYDROXY-2-[[[(PHENYLMETHYL)-OXY]-METHYL]-OXY]-6-HEPTEN-1-YL]-2,2-DIMETHYL-1,3-DIOXAN-4-YL]-METHYL]-2,2-
| 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 |