PALLADIUM-CATALYZED ACYLATION OF ORGANOZINCS AND OTHER ORGANOMETALLICS AS A CONVENIENT ROUTE TO KETONES

DOI: 10.1016/S0040-4039(00)88391-4

Source and publish data:

Tetrahedron Letters p. 5181 - 5184 (1983)

Update date:2022-08-02

Topics:

Authors:

Negishi, Ei-ichi

Bagheri, Vahid

Chatterjee, Sugata

Luo, Fen-Tair

Miller, Joseph A.

Stoll, A. Timothy

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Article abstract of DOI:10.1016/S0040-4039(00)88391-4

The reaction of organozincs with acyl chlorides catalyzed by palladium-phosphine complexes, e.g., Pd(PPh₃)₄, provides a highly general and convinient route to ketones.

Full text of DOI:10.1016/S0040-4039(00)88391-4

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