A novel ring cleavage reaction of oxazolines

Jeremy I. Levin, Steven M. Weinreb

Research output: Contribution to journalArticle

30 Citations (Scopus)

Abstract

An oxazoline can be cleanly converted to the parent carboxylic acid by treatment with NaOCl, followed by mild basic hydrolysis of the intermediate ester product(s).

Original languageEnglish (US)
Pages (from-to)2347-2350
Number of pages4
JournalTetrahedron Letters
Volume23
Issue number23
DOIs
StatePublished - Jan 1 1982

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Carboxylic Acids
Hydrolysis
Esters

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Drug Discovery
  • Organic Chemistry

Cite this

Levin, Jeremy I. ; Weinreb, Steven M. / A novel ring cleavage reaction of oxazolines. In: Tetrahedron Letters. 1982 ; Vol. 23, No. 23. pp. 2347-2350.
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A novel ring cleavage reaction of oxazolines. / Levin, Jeremy I.; Weinreb, Steven M.

In: Tetrahedron Letters, Vol. 23, No. 23, 01.01.1982, p. 2347-2350.

Research output: Contribution to journalArticle

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