The stereochemistry of reactions of 5 beta-androst-3-enes

Hanson J., Hitchcock P., Al-Jayyousi S., UYANIK C.

JOURNAL OF CHEMICAL RESEARCH-S, sa.8, ss.420-424, 1998 (SCI-Expanded, Scopus) identifier identifier

  • Yayın Türü: Makale / Tam Makale
  • Cilt numarası: Sayı: 8
  • Basım Tarihi: 1998
  • Doi Numarası: 10.1039/a800578h
  • Dergi Adı: JOURNAL OF CHEMICAL RESEARCH-S
  • Derginin Tarandığı İndeksler: Science Citation Index Expanded (SCI-EXPANDED), Scopus
  • Sayfa Sayıları: ss.420-424
  • Kocaeli Üniversitesi Adresli: Evet

Özet

Spectroscopic and crystallographic studies shows that the epoxidation, osmylation and bromination of 17 beta-acetoxy-5 beta-androst-3-ene takes place from the beta-face of the alkene and that a diequatorial dibromide and bromohydrin accompany the diaxial addition products.