ORGANO TIN NUCLEOPHILES IV. PALLADIUM CATALYZED CONJUGATE REDUCTION WITH TIN HYDRIDE

DOI: 10.1016/S0040-4039(00)86866-5

Source and publish data:

Tetrahedron Letters p. 477 - 480 (1982)

Update date:2022-08-04

Topics:

Authors:

Keinan, Ehud

Gleize, Pierre A.

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Article abstract of DOI:10.1016/S0040-4039(00)86866-5

Highly chemoselective conjugate reduction of α,β-unsaturated carbonyl compounds is now possible by using tributyl tin hydride with ; an optimization study puts forth the importance of added radical scavenger and proton source in these reductions.

Full text of DOI:10.1016/S0040-4039(00)86866-5

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