Ring expansion of steroid oxethans into hihydrooxazines

G. Schneider, László Hackler, P. Sohár

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

In tha case of oxethans condensed in an appropriate steric position to the sterane skeleton, the formation of six-membered dihydrooxazines has been observed with aliphatic or aromatic acid nitriles in the presence of Lewis acids, involving thus ring expansion.

Original languageEnglish
Pages (from-to)341-344
Number of pages4
JournalTetrahedron Letters
Volume22
Issue number4
DOIs
Publication statusPublished - 1981

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Lewis Acids
Nitriles
Carboxylic acids
Skeleton
Steroids
Acids

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Ring expansion of steroid oxethans into hihydrooxazines. / Schneider, G.; Hackler, László; Sohár, P.

In: Tetrahedron Letters, Vol. 22, No. 4, 1981, p. 341-344.

Research output: Contribution to journalArticle

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