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

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

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Cycloaddition
Cycloaddition Reaction
Skeleton
cephalotaxine

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 Letters, Vol. 35, No. 25, 20.06.1994, p. 4413-4414.

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 Letters. 1994 ; Vol. 35, No. 25. pp. 4413-4414.
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