A new method for the regioselective synthesis of β-enamino acid derivatives

DOI: 10.1016/S0040-4039(00)61664-7

Source and publish data:

Tetrahedron Letters p. 725 - 728 (1992)

Update date:2022-08-04

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Authors:

Fustero, Santos

Diaz, Ma. Dolores

Carlon, Raquel Perez

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Article abstract of DOI:10.1016/S0040-4039(00)61664-7

A mild, simple and efficient route to β-enamino imidazole carbonilic derivatives 3 by reaction of ketimines with N,N′-carbonyl diimidazole in the presence of boron triflouride as catalyst has been developed. The conversion of 3 to esters has also been explored.

Full text of DOI:10.1016/S0040-4039(00)61664-7

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