A DFT Study on the Mechanism of Palladium-Catalyzed Alkyne Hydrogenation: Neutral versus Cationic Pathways-Reference-Cited by-同舟云学术

A DFT Study on the Mechanism of Palladium-Catalyzed Alkyne Hydrogenation: Neutral versus Cationic Pathways

Published:2007-12-08 Issue:1 Volume:27 Page:43-52
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

López-Serrano Joaquín¹,Lledós Agustí¹,Duckett Simon B.¹

Affiliation:

1. Department of Chemistry, University of York, Heslington, YO10 5DD, York, United Kingdom, and Departament de Química, Universitat Autònoma de Barcelona, 08193 Barcelona, Spain

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om700307c

Reference59 articles.

1. Highly Selective Halide Anion-Promoted Palladium-Catalyzed Hydroformylation of Internal Alkenes to Linear Alcohols

2. Characterization and Dynamics of [Pd(L−L)H(solv)]+, [Pd(L−L)(CH2CH3)]+, and [Pd(L−L)(C(O)Et)(THF)]+ (L−L = 1,2-(CH2PBut2)2C6H4): Key Intermediates in the Catalytic Methoxycarbonylation of Ethene to Methylpropanoate

3. Ein neuer Katalysator für selektive Hydrierungen

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