1,3-dipolar cycloaddition approach towards the stereoselective preparation of aza-cephalotaxine skeleton

Miklós Nyerges, István Bitter, István Kádas, Gábor Tóth, László Toke

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

The aza-analogue of cephalotaxine skeleton has been prepared by series of reactions which include a 1,3-dipolar cycloaddition in 100% diastereoselectivity.

Original languageEnglish
Pages (from-to)4413-4414
Number of pages2
JournalTetrahedron Letters
Volume35
Issue number25
DOIs
Publication statusPublished - Jun 20 1994

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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