Use of the anomeric allylation reaction in natural products synthesis - a stereocontrolled synthesis of methyl deoxypseudomonate B.

Alan P. Kozikowski, Kirk L. Sorgi

Research output: Contribution to journalArticlepeer-review

Abstract

L-lyxose has been elaborated to methyl deoxypseudomonate B (I) by a sequence of reactions involving the Lewis acid catalyzed anomeric allylation procedure and a stereospecific Grignard addition reaction.

Original languageEnglish (US)
Pages (from-to)2085-2088
Number of pages4
JournalTetrahedron Letters
Volume25
Issue number20
DOIs
StatePublished - 1984

ASJC Scopus subject areas

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

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