Homochiral acetals in organic synthesis. A general enantioselective entry to carbohydrate derivatives from non-carbohydrate precursors

Eugene A Mash, Jeffrey B. Arterburn, James A. Fryling

Research output: Contribution to journalArticle

8 Citations (Scopus)

Abstract

A general chromatographic separation of furanosides and pyranosides derived from esters of lactic acid is disclosed. Application of this separation methodology to rapid syntheses of the diastereomers of (S)-methyl lactyl 4-deoxyribopyranose is described.

Original languageEnglish (US)
Pages (from-to)7145-7148
Number of pages4
JournalTetrahedron Letters
Volume30
Issue number51
DOIs
StatePublished - 1989

Fingerprint

Synthetic Chemistry Techniques
Acetals
Lactic Acid
Esters
Carbohydrates
Derivatives

ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

Homochiral acetals in organic synthesis. A general enantioselective entry to carbohydrate derivatives from non-carbohydrate precursors. / Mash, Eugene A; Arterburn, Jeffrey B.; Fryling, James A.

In: Tetrahedron Letters, Vol. 30, No. 51, 1989, p. 7145-7148.

Research output: Contribution to journalArticle

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