The influence of steric bulk on the geometry of triarylphosphite-based palladacycles and their tricyclohexylphosphine adducts-Reference-Cited by-同舟云学术

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The influence of steric bulk on the geometry of triarylphosphite-based palladacycles and their tricyclohexylphosphine adducts

Published:2006-03 Issue:4 Volume:25 Page:1003-1010
ISSN:0277-5387
Container-title:Polyhedron
language:en
Short-container-title:Polyhedron

Author:

Bedford Robin B.,Betham Michael,Coles Simon J.,Horton Peter N.,López-Sáez María-José

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Physical and Theoretical Chemistry

Reference21 articles.

1. Orthopalladated triaryl phosphite complexes as highly active catalysts in biaryl coupling reactions

2. Orthopalladated triarylphosphite complexes as highly efficient catalysts in the Heck reaction

3. Simple Mixed Tricyclohexylphosphane–Triarylphosphite Complexes as Extremely High-Activity Catalysts for the Suzuki Coupling of Aryl Chlorides

4. Extremely high activity catalysts for the Suzuki coupling of aryl chlorides: the importance of catalyst longevity

5. Simple tricyclohexylphosphine–palladium complexes as efficient catalysts for the Stille coupling of deactivated aryl chlorides

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2. An expedient approach to enhance Mizoroki-Heck coupling reaction by infrared irradiation using palladacycle compounds;Applied Organometallic Chemistry;2015-06-01

3. Synthesis of Substituted Biarylmethanol via Ferrocenyloxime Palladacycles Catalyzed Suzuki Reaction of Chlorophenylmethanol in Water;Bulletin of the Korean Chemical Society;2014-08-20

4. Five-membered cyclopalladated complex containing bidentate phosphine ligands; Synthesis, characterization, and highly efficient Suzuki cross-coupling reactions;Journal of Coordination Chemistry;2013-01-29

5. Orthometallated palladium trimers in C–C coupling reactions;Journal of Organometallic Chemistry;2012-07

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