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

Miklós Nyerges, I. Bitter, István Kádas, Gábor Tóth, L. Tőke

Research output: Contribution to journalArticle

21 Citations (Scopus)

Abstract

An aza-analogue of cephalotaxine 1 has been prepared stereoselectivly using 1,3-dipolar cycloaddition of azomethine ylide as a key step.

Original languageEnglish
Pages (from-to)11489-11502
Number of pages14
JournalTetrahedron
Volume51
Issue number42
DOIs
Publication statusPublished - Oct 16 1995

Fingerprint

Cycloaddition
Cycloaddition Reaction
Skeleton
cephalotaxine
azomethine

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

1,3-dipolar cycloaddition approach towards the stereoselective preparation of Aza-cephalotaxine skeleton. / Nyerges, Miklós; Bitter, I.; Kádas, István; Tóth, Gábor; Tőke, L.

In: Tetrahedron, Vol. 51, No. 42, 16.10.1995, p. 11489-11502.

Research output: Contribution to journalArticle

Nyerges, Miklós ; Bitter, I. ; Kádas, István ; Tóth, Gábor ; Tőke, L. / 1,3-dipolar cycloaddition approach towards the stereoselective preparation of Aza-cephalotaxine skeleton. In: Tetrahedron. 1995 ; Vol. 51, No. 42. pp. 11489-11502.
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