The dianion Claisen rearrangement of β-hydroxy esters

Mark J. Kurth, Chan Mo Yu

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Claisen rearrangement of β-hydroxy allylic ester dianions provides stereocontrolled access to three contiguous chiral centers on an acyclic framework; an unambiguous method has been developed for assessing diastereoselectivity.

Original languageEnglish (US)
Pages (from-to)5003-5006
Number of pages4
JournalTetrahedron Letters
Volume25
Issue number44
DOIs
StatePublished - 1984

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ASJC Scopus subject areas

  • Biochemistry
  • Organic Chemistry
  • Drug Discovery

Cite this

The dianion Claisen rearrangement of β-hydroxy esters. / Kurth, Mark J.; Yu, Chan Mo.

In: Tetrahedron Letters, Vol. 25, No. 44, 1984, p. 5003-5006.

Research output: Contribution to journalArticle

Kurth, Mark J. ; Yu, Chan Mo. / The dianion Claisen rearrangement of β-hydroxy esters. In: Tetrahedron Letters. 1984 ; Vol. 25, No. 44. pp. 5003-5006.
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