Michael addition reactions between various nucleophilic glycine equivalents and (S,E)-1-enoyl-5-oxo-N-phenylpyrrolidine-2-carboxamide, an optimal type of chiral Michael acceptor in the asymmetric synthesis of β-phenyl pyroglutamic acid and related compounds

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Title
Michael addition reactions between various nucleophilic glycine equivalents and (S,E)-1-enoyl-5-oxo-N-phenylpyrrolidine-2-carboxamide, an optimal type of chiral Michael acceptor in the asymmetric synthesis of β-phenyl pyroglutamic acid and related compounds
Authors
Keywords
-
Journal
TETRAHEDRON-ASYMMETRY
Volume 20, Issue 22, Pages 2629-2634
Publisher
Elsevier BV
Online
2009-11-12
DOI
10.1016/j.tetasy.2009.10.006

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