THE CONTROL OF DIASTEREOSELECTIVITY IN THE MICHAEL REACTION OF KETONIC ENOLATES WITH CROTONIC ACID DERIVATIVES

DOI: 10.1016/S0040-4039(00)60431-8

Source and publish data:

Tetrahedron Letters p. 2421 - 2424 (1993)

Update date:2022-09-26

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Authors:

Corey, E. J.

Houpis, Ioannis N.

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Article abstract of DOI:10.1016/S0040-4039(00)60431-8

Methodology is described for the selective generation of either anti or syn Michael adducts from various ketone enolates and crotonic ester 18 or amide 15.

Full text of DOI:10.1016/S0040-4039(00)60431-8

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