20-[(1'R)-HYDROXY-(2'R)-TRIFLUOROMETHYL-3'-BUTEN-1'-YL]-3-OXOPREGN-4-ENE
Compound with spectra: 1 NMR
![20-[(1'R)-HYDROXY-(2'R)-TRIFLUOROMETHYL-3'-BUTEN-1'-YL]-3-OXOPREGN-4-ENE](/api/compound/LT9NveCoeTA.png?ph=true&h=300&w=458 "20-[(1'R)-HYDROXY-(2'R)-TRIFLUOROMETHYL-3'-BUTEN-1'-YL]-3-OXOPREGN-4-ENE")
| SpectraBase Compound ID | LT9NveCoeTA |
|---|---|
| InChI | InChI=1S/C26H37F3O2/c1-5-19(26(27,28)29)23(31)15(2)20-8-9-21-18-7-6-16-14-17(30)10-12-24(16,3)22(18)11-13-25(20,21)4/h5,14-15,18-23,31H,1,6-13H2,2-4H3/t15-,18-,19-,20+,21?,22?,23-,24?,25?/m0/s1 |
| InChIKey | MKKSZEQWIIQNIY-GHNDNMSYSA-N |
| Mol Weight | 438.6 g/mol |
| Molecular Formula | C26H37F3O2 |
| Exact Mass | 438.274565 g/mol |
| Enantiomer InChIKey | MKKSZEQWIIQNIY-VXOGGIPGSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
3-OXO-23,24-DINORCHOL-4-ENE-22-HYDROXY-ACID;MAJOR-DIASTEREOMER
HALOSTEROL-A;(22R,24R)-24-ETHYL-3-OXOCHOLEST-4-EN-22-OL
3-OXO-23,24-DINORCHOL-4-ENE-22-CYANOHYDRIN-SILYL-ETHER;MAJOR-DIASTEREOMER
(22R or 22S)-22-Trimethylsilyloxy-4-cholesten-3-one
No Name
Cholest-4-en-26-oic acid, 22-hydroxy-3-oxo-, .delta.-lactone, (22R,25S)-
(+)-(20-S)-20-O-LAUROYLPREGN-4-EN-3-ONE
(22E,24-ALPHA)-24-ETHYL-3-OXO-CHOLESTA-4,22(23)-DIEN-25-OL
(+)-(20-S)-20-O-MYRISTOLPREGN-4-EN-3-ONE
(+)-(20-S)-20-O-CAPRINOYLPREGN-4-EN-3-ONE
| Title | Journal or Book | Year |
|---|---|---|
| Stereocontrolled Synthesis of Linear 22R-Homoallylic Sterols via a Triflic Acid-Catalyzed 2-Oxonia Cope Rearrangement | Organic Letters | 2002 |