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 journalArticle

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
Externally publishedYes

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Allylation
Lewis Acids
Addition reactions
Biological Products
lyxose

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Use of the anomeric allylation reaction in natural products synthesis - a stereocontrolled synthesis of methyl deoxypseudomonate B. / Kozikowski, Alan P.; Sorgi, Kirk L.

In: Tetrahedron Letters, Vol. 25, No. 20, 1984, p. 2085-2088.

Research output: Contribution to journalArticle

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