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Synthesis 2007(1): 113-117
DOI: 10.1055/s-2006-958929
DOI: 10.1055/s-2006-958929
PAPER
© Georg Thieme Verlag Stuttgart · New York
A Facile Synthesis of Ethyl 2-Acetamido-4-methylenehex-5-enoate, a Versatile Diels-Alder Synthon for the Parallel Synthesis of Novel α-Amino Acid Derivatives
Further Information
Received
7 August 2006
Publication Date:
12 December 2006 (online)
Publication History
Publication Date:
12 December 2006 (online)
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Abstract
An efficient synthesis of a diene-containing α-amino acid via the use of Denmark’s coupling reaction and its application to the synthesis of novel α-amino acid via the Diels-Alder reaction are described.
Key words
amino acid - diene - Diels-Alder - palladium - coupling
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