Enantiospecific synthesis of (3s-hydroxy-2s-methyl) butyltriphenylphosphonium iodide, a precursor for the chiral side chain of pseudomonic acid C

G. W.J. Fleet, Tony Kung Ming Shing

Research output: Contribution to journalArticle

14 Citations (Scopus)

Abstract

The enantiospecific synthesis of (3S-hydroxy-2S-methyl)butyl triphenylphosphonium iodide from L-arabinose is described.

Original languageEnglish
Pages (from-to)3657-3660
Number of pages4
JournalTetrahedron Letters
Volume24
Issue number34
DOIs
Publication statusPublished - 1983 Jan 1
Externally publishedYes

Fingerprint

Mupirocin
Arabinose
Iodides
methyl iodide
butyltriphenylphosphonium

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Enantiospecific synthesis of (3s-hydroxy-2s-methyl) butyltriphenylphosphonium iodide, a precursor for the chiral side chain of pseudomonic acid C. / Fleet, G. W.J.; Shing, Tony Kung Ming.

In: Tetrahedron Letters, Vol. 24, No. 34, 01.01.1983, p. 3657-3660.

Research output: Contribution to journalArticle

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