Fluoride Ion Mediated Peterson Alkenation of N-amido Derivatives with Carbonyl Compounds: A Short General Route to Enamides and 1,2-Dihydroisoquinolines

DOI: 10.1016/S0040-4039(00)74815-5

Source and publish data:

Tetrahedron Letters p. 3903 - 3906 (1992)

Update date:2022-08-03

Topics:

Authors:

Palomo, Claudio

Aizpurua, Jesus M.

Legido, Marta

Picard, Jean Paul

Dunogues, Jacques

Constantieux, Thierry

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Article abstract of DOI:10.1016/S0040-4039(00)74815-5

A straighforward general access to diversely substituted acyclic or cyclic enamides and dienamides is accomplished by using a fluoride induced Peterson olefination of carbonyl compounds and enolizable amides derived from C,C-bis(trimethylsilyl)methylamine

Full text of DOI:10.1016/S0040-4039(00)74815-5

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