A CYANIDE PROMOTED MICHAEL REACTION: THE USE OF AN AMINONITRILE AS AN ENAMINE EQUIVALENT FOR THE MICHAEL REACTION

DOI: 10.1016/S0040-4039(00)88452-X

Source and publish data:

Tetrahedron Letters p. 6831 - 6834 (1988)

Update date:2022-08-04

Topics:: Authors:

Mitch, Charles H.

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Article abstract of DOI:10.1016/S0040-4039(00)88452-X

An enamine lacking a beta-proton is shown to undergo the Michael reaction if the intermediate iminium ion is trapped with a nucleophile, such as cyanide.Reductive cleavage of the resulting nitrile affords an aminoketone product.

Full text of DOI:10.1016/S0040-4039(00)88452-X

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Article Doi

A CYANIDE PROMOTED MICHAEL REACTION: THE USE OF AN AMINONITRILE AS AN ENAMINE EQUIVALENT FOR THE MICHAEL REACTION

DOI: 10.1016/S0040-4039(00)88452-X

Source and publish data:

Authors:

Article abstract of DOI:10.1016/S0040-4039(00)88452-X

Full text of DOI:10.1016/S0040-4039(00)88452-X

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