Dianion of N-Phenyl-2-propenamide as a Versatile Reagent for the Preparation of α-Methylene Carbonyl Compounds

DOI: 10.1021/jo00262a020

Source and publish data:

Journal of Organic Chemistry p. 63 - 70 (1989)

Update date:2022-08-05

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Authors:

Tanaka, Kazuhiko

Horiuchi, Hiroshi

Yoda, Hidemi

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Article abstract of DOI:10.1021/jo00262a020

A general synthetic route to α-methylene β-lactams is described that involves the regioselective electrophilic substitution of the dianion 2 generated from N-phenyl-2-<(phenylsulfonyl)methyl>propenamide (1).A convergent synthesis of conocandin N-phenylami

Full text of DOI:10.1021/jo00262a020

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