Issue 5, 1987
From the journal:

Journal of the Chemical Society, Chemical Communications

Regioselective palladium-catalysed amination of 4-chloroacetoxyalk-2-enoic esters: synthesis of pyrrol-2(5H)-ones (4-but-2-enelactams)

Rikuhei Tanikaga,   Jun Takeuchi,   Masayuki Takyu  and  Aritsune Kaji  

Abstract

Palladium(0)-catalysed reactions of 4-chloroacetoxyalk-2-enoic esters with amines selectively give 4-aminoalk-2-enoic esters, which are readily converted into pyrrol-2(5H)-ones (4-but-2-enelactams).

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Article information

DOI
https://doi.org/10.1039/C39870000386
Article type
Paper

J. Chem. Soc., Chem. Commun., 1987, 386-387

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Regioselective palladium-catalysed amination of 4-chloroacetoxyalk-2-enoic esters: synthesis of pyrrol-2(5H)-ones (4-but-2-enelactams)

R. Tanikaga, J. Takeuchi, M. Takyu and A. Kaji, J. Chem. Soc., Chem. Commun., 1987, 386 DOI: 10.1039/C39870000386

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