Palladium-catalyzed conjugate reduction of α-β-unsaturated carbonyl compound with tributyltin hydride. The promoting influence of the presence of protonic or lewis acids.-Reference-Cited by-同舟云学术

Palladium-catalyzed conjugate reduction of α-β-unsaturated carbonyl compound with tributyltin hydride. The promoting influence of the presence of protonic or lewis acids.

Published:1982-01 Issue:17 Volume:23 Page:1825-1828
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Four P.,Guibe P.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference15 articles.

1. Palladium-catalysed reaction of tributyltin hydride with acyl chlorides. A selective route to aldehydes

2. Palladium-catalyzed reaction of tributyltin hydride with acyl chlorides. A mild, selective, and general route to aldehydes

3. The allyloxycarbonyl group for alcohol protection: quantitative removal or transformation into allyl protecting group via π-allyl complexes of palladium

4. Organo tin nucleophiles iii. Palladium catalyzed reductive cleavage of allylic heterosubstituents with tin hydride

5. Organo tin nucleophiles IV. Palladium catalyzed conjugate reduction with tin hydride

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