Configurational analysis of 16-methyl-androstene-5 derivatives

Gy Schnneider, E. Meskó, L. Hackler, G. Dombi, D. Zeigan, G. Engelhardt

Research output: Contribution to journalArticle

5 Citations (Scopus)

Abstract

The four possible isomers of 16-hydroxymethyl-androst-5-ene-3β,17-diol were converted into the corresponding 16-methyl analogues characterized by 13C-NMR and 1H-NMR spectra. This made possible the configurational correlation of 16-methylandrost-5-ene derivatives described in the literature.

Original languageEnglish
Pages (from-to)1205-1211
Number of pages7
JournalTetrahedron
Volume40
Issue number7
DOIs
Publication statusPublished - 1984

Fingerprint

Androstenediol
Androstenes
Nuclear magnetic resonance
Derivatives
Isomers
16-androstene
Carbon-13 Magnetic Resonance Spectroscopy
Proton Magnetic Resonance Spectroscopy

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Schnneider, G., Meskó, E., Hackler, L., Dombi, G., Zeigan, D., & Engelhardt, G. (1984). Configurational analysis of 16-methyl-androstene-5 derivatives. Tetrahedron, 40(7), 1205-1211. https://doi.org/10.1016/S0040-4020(01)99328-7

Configurational analysis of 16-methyl-androstene-5 derivatives. / Schnneider, Gy; Meskó, E.; Hackler, L.; Dombi, G.; Zeigan, D.; Engelhardt, G.

In: Tetrahedron, Vol. 40, No. 7, 1984, p. 1205-1211.

Research output: Contribution to journalArticle

Schnneider, G, Meskó, E, Hackler, L, Dombi, G, Zeigan, D & Engelhardt, G 1984, 'Configurational analysis of 16-methyl-androstene-5 derivatives', Tetrahedron, vol. 40, no. 7, pp. 1205-1211. https://doi.org/10.1016/S0040-4020(01)99328-7
Schnneider G, Meskó E, Hackler L, Dombi G, Zeigan D, Engelhardt G. Configurational analysis of 16-methyl-androstene-5 derivatives. Tetrahedron. 1984;40(7):1205-1211. https://doi.org/10.1016/S0040-4020(01)99328-7
Schnneider, Gy ; Meskó, E. ; Hackler, L. ; Dombi, G. ; Zeigan, D. ; Engelhardt, G. / Configurational analysis of 16-methyl-androstene-5 derivatives. In: Tetrahedron. 1984 ; Vol. 40, No. 7. pp. 1205-1211.
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