Literature DB >> 16494457

Oxidative addition of phenyl bromide to Pd(BINAP) vs Pd(BINAP)(amine). Evidence for addition to Pd(BINAP).

Shashank Shekhar1, Per Ryberg, John F Hartwig.   

Abstract

The rates of oxidative addition of phenyl bromide to [Pd(BINAP)2] have been measured in the presence and absence of added amine to assess a previous hypothesis that addition to [Pd(BINAP)(amine)] is faster than addition to [Pd(BINAP)]. These data show that addition to the amine complex is not faster than addition to [Pd(BINAP)]. Instead, they are consistent with oxidative addition, even in the presence of amine, to [Pd(BINAP)] as the major pathway. These data underscore the value of studying the stoichiometric reactions of isolated complexes when assessing the mechanism of a catalytic process.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 16494457     DOI: 10.1021/ol0528890

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Effect of ligand steric properties and halide identity on the mechanism for oxidative addition of haloarenes to trialkylphosphine Pd(0) complexes.

Authors:  Fabiola Barrios-Landeros; Brad P Carrow; John F Hartwig
Journal:  J Am Chem Soc       Date:  2009-06-17       Impact factor: 15.419

2.  Pd-Catalyzed C-N Coupling Reactions Facilitated by Organic Bases: Mechanistic Investigation Leads to Enhanced Reactivity in the Arylation of Weakly Binding Amines.

Authors:  Joseph M Dennis; Nicholas A White; Richard Y Liu; Stephen L Buchwald
Journal:  ACS Catal       Date:  2019-03-15       Impact factor: 13.084

3.  Synthetic and mechanistic studies on Pd(0)-catalyzed diamination of conjugated dienes.

Authors:  Baoguo Zhao; Haifeng Du; Sunliang Cui; Yian Shi
Journal:  J Am Chem Soc       Date:  2010-03-17       Impact factor: 15.419

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.