Use of π-allylpalladium as a nucleophile via an alkyl-allyl exchange reaction with alkylzinc

DOI: 10.1016/S0040-4039(00)60415-X

Source and publish data:

Tetrahedron Letters p. 7619 - 7622 (1993)

Update date:2022-08-29

Topics:

Authors:

Yasui, Kengo

Goto, Youichi

Yajima, Takafumi

Taniseki, Yasue

Fugami, Keigo

Tanaka, Akihiro

Tamaru, Yoshinao

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Article abstract of DOI:10.1016/S0040-4039(00)60415-X

Allylation of carbonyl compounds (aldehydes, ketones, esters, lactones, acid anhydrides) proceeds smoothly at room temperature by the reaction of a carbonyl compound, an allylic benzoate or allylic phenyl ether, diethylzinc, and a catalytic amount of Pd(0

Full text of DOI:10.1016/S0040-4039(00)60415-X

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