Reductive cyclization of δ-hydroxy nitriles

A new synthesis of glycosylamines

Andrew D. Dorsey, Jennifer E. Barbarow, Dirk Trauner

Research output: Contribution to journalArticle

Abstract

(Matrix presented) The stereoselective cyclization of δ-hydroxy nitriles to afford N,O-acetals and the application of this reaction toward the synthesis of glycosylamines is described.

Original languageEnglish (US)
Pages (from-to)3237-3239
Number of pages3
JournalOrganic Letters
Volume5
Issue number18
DOIs
StatePublished - Sep 4 2003

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acetals
Acetals
Nitriles
Cyclization
nitriles
synthesis
matrices

ASJC Scopus subject areas

  • Biochemistry
  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Reductive cyclization of δ-hydroxy nitriles : A new synthesis of glycosylamines. / Dorsey, Andrew D.; Barbarow, Jennifer E.; Trauner, Dirk.

In: Organic Letters, Vol. 5, No. 18, 04.09.2003, p. 3237-3239.

Research output: Contribution to journalArticle

Dorsey, Andrew D. ; Barbarow, Jennifer E. ; Trauner, Dirk. / Reductive cyclization of δ-hydroxy nitriles : A new synthesis of glycosylamines. In: Organic Letters. 2003 ; Vol. 5, No. 18. pp. 3237-3239.
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