Pd-catalysed methoxycarbonylation of vinylarenes using chiral monodentate phosphetanes and phospholane as ligands. Effect of substrate substituents on enantioselectivity-Reference-Cited by-同舟云学术

Pd-catalysed methoxycarbonylation of vinylarenes using chiral monodentate phosphetanes and phospholane as ligands. Effect of substrate substituents on enantioselectivity

Published:2007 Issue:47 Volume: Page:5524
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Muñoz Bianca K.,Godard Cyril,Marinetti Angela,Ruiz Aurora,Benet-Buchholz Jordi,Claver Carmen

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2007/DT/B705230H

Reference51 articles.

1. Highly active and selective palladium catalyst for hydroesterification of styrene and vinyl acetate promoted by polymeric sulfonic acids

2. Electronic Effect of Diphosphines on the Regioselectivity of the Palladium-Catalyzed Hydroesterification of Styrene

3. Chiral Monophosphines as Ligands for Asymmetric Organometallic Catalysis.

4. Asymmetric induction in carbonmethoxylation of vinylaromatics

5. Hydroesterification of styrene catalyzed by montmorillonite-diphenylphosphinepalladium(II) chloride in the presence of chiral phosphines

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