ORGANO TIN NUCLEOPHILES III. PALLADIUM CATALYZED REDUCTIVE CLEAVAGE OF ALLYLIC HETEROSUBSTITUENTS WITH TIN HYDRIDE

DOI: 10.1016/S0040-4039(00)86797-0

Source and publish data:

Tetrahedron Letters p. 241 - 244 (1982)

Update date:2022-08-02

Topics:

Authors:

Keinan, Ehud

Greenspoon, Noam

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Article abstract of DOI:10.1016/S0040-4039(00)86797-0

Tributyl tin hydride, serving as an efficient hydride transfer agent, allows highly chemoselective palladium catalyzed reductions of allylic heterosubstituents even in presence of aldehydes, benzyl acetate and benzyl chloride.

Full text of DOI:10.1016/S0040-4039(00)86797-0

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