Published 1981
| Version v1
Journal article
Stereoselective reduction of a hydroxymethylene keto steroid
- 1. Jozsef Attila Tudomanyegyetem, Szeged (Hungary)
Description
15-Formyl-16-keto-3β,17β-di-(2'-tetrahydropyranyloxy)-5-androstene was reduced stereoselectively to the 15α-hydroxymethyl-16β-hydroxy derivative; chemical and 1H-NMR evidence for the steric structures of the compounds are given. (author)
Additional details
Publishing Information
- Journal Title
- Acta Chim. Acad. Sci. Hung.
- Journal Volume
- 106
- Journal Issue
- 4
- Series
- Acta Chim. Acad. Sci. Hung.
- Journal Page Range
- 359-361
- ISSN
- 0001-5407
INIS
- Country of Publication
- Hungary
- Country of Input or Organization
- Hungary
- INIS RN
- 12633518
- Subject category
- S75: CONDENSED MATTER PHYSICS, SUPERCONDUCTIVITY AND SUPERFLUIDITY;
- Descriptors DEI
- ANDROSTANES; MOLECULAR STRUCTURE; NUCLEAR MAGNETIC RESONANCE; REDUCTION; STEREOCHEMISTRY; STRUCTURAL CHEMICAL ANALYSIS
- Descriptors DEC
- CHEMICAL REACTIONS; MAGNETIC RESONANCE; ORGANIC COMPOUNDS; RESONANCE; STEROIDS
Optional Information
- Notes
- 4 refs.