Macrocyclisation: The tin directed reaction of a carbohydrate derivative with succinyl chloride

Mathys M. Basson, Martin W. Bredenkamp, Cedric W. Holzapfel

Research output: Contribution to journalArticlepeer-review

3 Citations (Scopus)

Abstract

Condensation of methyl 4,6-O-benzylidene-2,3-O-dibutylstanylene-α-D-glucopyranoside with succinyl chloride furnished two macrocyclic tetralactones, a hexalactone and an octalactone.

Original languageEnglish
Pages (from-to)591-594
Number of pages4
JournalTetrahedron Letters
Volume30
Issue number5
DOIs
Publication statusPublished - 1989

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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