5-(HYDROXYMETHYL)-6-EPSILON-METHYL-3-BETA-[(METHYLMERCURIO)-METHYL]-A,B-BISNOR-5-BETA-CHOLESTANE;MAJOR-ISOMER
Compound with spectra: 1 NMR
![5-(HYDROXYMETHYL)-6-EPSILON-METHYL-3-BETA-[(METHYLMERCURIO)-METHYL]-A,B-BISNOR-5-BETA-CHOLESTANE;MAJOR-ISOMER](/api/compound/EQl02Q9Jrbg.png?ph=true&h=300&w=458 "5-(HYDROXYMETHYL)-6-EPSILON-METHYL-3-BETA-[(METHYLMERCURIO)-METHYL]-A,B-BISNOR-5-BETA-CHOLESTANE;MAJOR-ISOMER")
| SpectraBase Compound ID | EQl02Q9Jrbg |
|---|---|
| InChI | InChI=1S/C28H49O.CH3.Hg/c1-18(2)9-8-10-19(3)23-11-12-24-22-17-28(21(5)29)20(4)13-16-27(28,7)25(22)14-15-26(23,24)6;;/h18-25,29H,4,8-17H2,1-3,5-7H3;1H3;/t19-,20+,21-,22+,23-,24+,25+,26-,27-,28-;;/m1../s1 |
| InChIKey | FQBLPUIKLXGACD-KVOJPWMWSA-N |
| Mol Weight | 617.3 g/mol |
| Molecular Formula | C29H52HgO |
| Exact Mass | 618.37246 g/mol |
| Enantiomer InChIKey | FQBLPUIKLXGACD-NXNJXWMNSA-N |
| Copyright | Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved. |
|---|---|
| Solvent | CDCl3 |
5-(Hydroxymethyl)-A,B-bisnor-3.beta.-[(methylmercurio)methyl]-5.beta.-cholestane
5-(HYDROXYMETHYL)-3-BETA-[(METHYLMERCURIO)-METHYL]-A,B-BISNOR-5-BETA-CHOLESTANE
3-BETA-[(BROMOMERCURIO)-METHYL]-A,B-BISNOR-5-BETA-CHOLESTANE-5-CARBALDEHYDE
3-BETA-((BROMOMERCURIO)-METHYL)-A,B-DINOR-5-BETA-CHOLESTANE-5-CARBALDEHYDE
3-BETA-[(BROMOMERCURIO)-METHYL]-5-(HYDROXYMETHYL)-A,B-BISNOR-5-BETA-CHOLESTANE
B-NOR-4-BETA,5-BETA-METHANO-CHOLESTAN-3-ONE
(24Z)-STIGMAST-24(28)-ENE-3-BETA,5-ALPHA,6-BETA-TRIOL
Cholestane-3.beta.,5.alpha.,6.beta.,26-tetrol - 26-Acetate
25.psi.-Cholestane-3.beta.,5.alpha.,6.beta.,26-tetrol - 26-Acetate
25-XI-CHOLESTANE-3-BETA,5-ALPHA,6-BETA,26-TETRAOL-26-ACETATE
| Title | Journal or Book | Year |
|---|---|---|
| An Approach toward the Triquinane-Type Skeleton via Reagent-Controlled Skeletal Rearrangements. A Facile Method for Protection−Deprotection of Organomercurials, Tuning the Selectivity of Wagner−Meerwein Migrations, and a New Route to Annulated Lactones | The Journal of Organic Chemistry | 1998 |