Palladium-catalyzed synthesis of β-lactams via carbonylative cycloaddition of benzyl and allyl halides with imines

Article abstract of DOI:10.1080/00397919908086431

Benzyl and allyl halides rect stereoselectively with imines under carbon monoxide pressure in the presence of a catalytic amount of bis(triphenylphosphine)palladium(II) chloride together with triethylamine to afford the corresponding β-lactams in good yields.

Full text of DOI:10.1080/00397919908086431

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Synthetic Communications: An
International Journal for Rapid
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Palladium-Catalyzed Synthesis
of β-Lactams via Carbonylative
Cycloaddition of Benzyl and Allyl
Halides with Imines
Chan Sik Cho a , Li Hong Jiang a & Sang Chul Shim a
a Department of Industrial Chemistry , College of
Engineering, Kyungpook National University , Taegu,
702-701, Korea
Published online: 25 Sep 2007.
To cite this article: Chan Sik Cho , Li Hong Jiang & Sang Chul Shim (1999) Palladium-
Catalyzed Synthesis of β-Lactams via Carbonylative Cycloaddition of Benzyl and Allyl Halides
with Imines, Synthetic Communications: An International Journal for Rapid Communication of
Synthetic Organic Chemistry, 29:15, 2695-2703, DOI: 10.1080/00397919908086431
To link to this article: http://dx.doi.org/10.1080/00397919908086431
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