Enantioselective total and formal syntheses of paroxetine (PAXIL) via phosphine-catalyzed enone α-arylation using arylbismuth(V) reagents: a regiochemical complement to Heck arylation-Reference-Cited by-同舟云学术

Enantioselective total and formal syntheses of paroxetine (PAXIL) via phosphine-catalyzed enone α-arylation using arylbismuth(V) reagents: a regiochemical complement to Heck arylation

Published:2006-11 Issue:45 Volume:62 Page:10594-10602
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Koech Phillip K.,Krische Michael J.

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference100 articles.

1. For selected monographs encompassing Lewis base catalysis, see:

2. Enantioselective Organocatalysis

3. Asymmetric Organocatalysis;Berkessel,2005

4. For phosphine-catalyzed regioretentive allylic substitutions of Morita–Baylis–Hillman acetates, see:

5. Phosphine-Catalyzed Regiospecific Allylic Amination and Dynamic Kinetic Resolution of Morita−Baylis−Hillman Acetates

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