An Ireland–Claisen rearrangement approach to β2,3-amino acids

Paul M Ylioja, Alexander D Mosley, Claire E Charlot, David R Carbery

Research output: Contribution to journalArticle

29 Citations (Scopus)

Abstract

The first use of enamide substrates in an Ireland–Claisen [3,3]-sigmatropic rearrangement reaction is presented as a novel route to complex β2,3-amino acids
Original languageEnglish
Pages (from-to)1111-1114
Number of pages4
JournalTetrahedron Letters
Volume49
Issue number7
DOIs
Publication statusPublished - 2008

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Amino Acids
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An Ireland–Claisen rearrangement approach to β2,3-amino acids. / Ylioja, Paul M; Mosley, Alexander D; Charlot, Claire E; Carbery, David R.

In: Tetrahedron Letters, Vol. 49, No. 7, 2008, p. 1111-1114.

Research output: Contribution to journalArticle

Ylioja, Paul M ; Mosley, Alexander D ; Charlot, Claire E ; Carbery, David R. / An Ireland–Claisen rearrangement approach to β2,3-amino acids. In: Tetrahedron Letters. 2008 ; Vol. 49, No. 7. pp. 1111-1114.
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