Literature DB >> 28266847

Structural, Kinetic, and Computational Characterization of the Elusive Arylpalladium(II)boronate Complexes in the Suzuki-Miyaura Reaction.

Andy A Thomas1, Hao Wang1, Andrew F Zahrt1, Scott E Denmark1.   

Abstract

The existence of the oft-invoked intermediates containing the crucial Pd-O-B subunit, the "missing link", has been established in the Suzuki-Miyaura cross-coupling reaction. The use of low-temperature, rapid injection NMR spectroscopy (RI-NMR), kinetic studies, and computational analysis has enabled the generation, observation, and characterization of these highly elusive species. The ability to confirm the intermediacy of Pd-O-B-containing species provided the opportunity to clarify mechanistic aspects of the transfer of the organic moiety from boron to palladium in the key transmetalation step. Specifically, these studies establish the identity of two different intermediates containing Pd-O-B linkages, a tri-coordinate (6-B-3) boronic acid complex and a tetra-coordinate (8-B-4) boronate complex, both of which undergo transmetalation leading to the cross-coupling product. Two distinct mechanistic pathways have been elucidated for stoichiometric reactions of these complexes: (1) transmetalation via an unactivated 6-B-3 intermediate that dominates in the presence of an excess of ligand, and (2) transmetalation via an activated 8-B-4 intermediate that takes place with a deficiency of ligand.

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Year:  2017        PMID: 28266847      PMCID: PMC7784246          DOI: 10.1021/jacs.6b13384

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  29 in total

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Journal:  Inorg Chem       Date:  2005-10-31       Impact factor: 5.165

2.  Palladium-catalyzed cross-coupling: a historical contextual perspective to the 2010 Nobel Prize.

Authors:  Carin C C Johansson Seechurn; Matthew O Kitching; Thomas J Colacot; Victor Snieckus
Journal:  Angew Chem Int Ed Engl       Date:  2012-05-09       Impact factor: 15.336

3.  Selection of boron reagents for Suzuki-Miyaura coupling.

Authors:  Alastair J J Lennox; Guy C Lloyd-Jones
Journal:  Chem Soc Rev       Date:  2013-10-03       Impact factor: 54.564

4.  Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms.

Authors:  Vilas B Phapale; Diego J Cárdenas
Journal:  Chem Soc Rev       Date:  2009-03-17       Impact factor: 54.564

5.  Kinetic data for the transmetalation/reductive elimination in palladium-catalyzed Suzuki-Miyaura reactions: unexpected triple role of hydroxide ions used as base.

Authors:  Christian Amatore; Anny Jutand; Gaëtan Le Duc
Journal:  Chemistry       Date:  2011-01-17       Impact factor: 5.236

6.  Cross-coupling reactions of organoboranes: an easy way to construct C-C bonds (Nobel Lecture).

Authors:  Akira Suzuki
Journal:  Angew Chem Int Ed Engl       Date:  2011-05-25       Impact factor: 15.336

7.  Probing the Electronic Demands of Transmetalation in the Palladium-Catalyzed Cross-Coupling of Arylsilanolates.

Authors:  Scott E Denmark; Russell C Smith; Wen-Tau T Chang
Journal:  Tetrahedron       Date:  2011-06-17       Impact factor: 2.457

8.  Aryl trifluoroborates in Suzuki-Miyaura coupling: the roles of endogenous aryl boronic acid and fluoride.

Authors:  Mike Butters; Jeremy N Harvey; Jesus Jover; Alastair J J Lennox; Guy C Lloyd-Jones; Paul M Murray
Journal:  Angew Chem Int Ed Engl       Date:  2010-07-12       Impact factor: 15.336

9.  Pre-transmetalation intermediates in the Suzuki-Miyaura reaction revealed: The missing link.

Authors:  Andy A Thomas; Scott E Denmark
Journal:  Science       Date:  2016-04-15       Impact factor: 47.728

10.  Distinct electronic effects on reductive eliminations of symmetrical and unsymmetrical bis-aryl platinum complexes.

Authors:  Shashank Shekhar; John F Hartwig
Journal:  J Am Chem Soc       Date:  2004-10-13       Impact factor: 15.419

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  12 in total

1.  Anhydrous, Homogeneous, Suzuki-Miyaura Cross-Coupling of Boronic Esters using Potassium Trimethylsilanolate.

Authors:  Connor P Delaney; Ethan M Heyboer; Scott E Denmark
Journal:  Organic Synth       Date:  2020-09-08

2.  DFT Investigation of Suzuki-Miyaura Reactions with Aryl Sulfamates Using a Dialkylbiarylphosphine-Ligated Palladium Catalyst.

Authors:  Patrick R Melvin; Ainara Nova; David Balcells; Nilay Hazari; Mats Tilset
Journal:  Organometallics       Date:  2017-09-13       Impact factor: 3.876

3.  Enantioselective Construction of Tertiary Boronic Esters by Conjunctive Cross-Coupling.

Authors:  Jesse A Myhill; Liang Zhang; Gabriel J Lovinger; James P Morken
Journal:  Angew Chem Int Ed Engl       Date:  2018-08-29       Impact factor: 15.336

4.  Potassium Trimethylsilanolate Enables Rapid, Homogeneous Suzuki-Miyaura Cross-Coupling of Boronic Esters.

Authors:  Connor P Delaney; Vincent M Kassel; Scott E Denmark
Journal:  ACS Catal       Date:  2019-12-02       Impact factor: 13.084

5.  Elucidating the Role of the Boronic Esters in the Suzuki-Miyaura Reaction: Structural, Kinetic, and Computational Investigations.

Authors:  Andy A Thomas; Andrew F Zahrt; Connor P Delaney; Scott E Denmark
Journal:  J Am Chem Soc       Date:  2018-03-15       Impact factor: 15.419

6.  Computationally Assisted Mechanistic Investigation and Development of Pd-Catalyzed Asymmetric Suzuki-Miyaura and Negishi Cross-Coupling Reactions for Tetra-ortho-Substituted Biaryl Synthesis.

Authors:  Nitinchandra Dahyabhai Patel; Joshua D Sieber; Sergei Tcyrulnikov; Bryan J Simmons; Daniel Rivalti; Krishnaja Duvvuri; Yongda Zhang; Donghong A Gao; Keith R Fandrick; Nizar Haddad; Kendricks So Lao; Hari Prasad Reddy Mangunuru; Soumik Biswas; Bo Qu; Nelu Grinberg; Scott Pennino; Heewon Lee; Jinhua J Song; B Frank Gupton; Neil K Garg; Marisa C Kozlowski; Chris H Senanayake
Journal:  ACS Catal       Date:  2018-09-20       Impact factor: 13.084

7.  Asymmetric synthesis via stereospecific C-N and C-O bond activation of alkyl amine and alcohol derivatives.

Authors:  Sarah M Pound; Mary P Watson
Journal:  Chem Commun (Camb)       Date:  2018-10-30       Impact factor: 6.222

8.  Aryl Amination Using Soluble Weak Base Enabled by a Water-Assisted Mechanism.

Authors:  Sii Hong Lau; Peng Yu; Liye Chen; Christina B Madsen-Duggan; Michael J Williams; Brad P Carrow
Journal:  J Am Chem Soc       Date:  2020-11-12       Impact factor: 15.419

9.  Diastereoselective and Enantioselective Conjunctive Cross-Coupling Enabled by Boron Ligand Design.

Authors:  Jesse A Myhill; Christopher A Wilhelmsen; Liang Zhang; James P Morken
Journal:  J Am Chem Soc       Date:  2018-11-06       Impact factor: 15.419

10.  Diastereo- and Enantioselective 1,4-Difunctionalization of Borylenynes by Catalytic Conjunctive Cross-Coupling.

Authors:  Chunyin Law; Elton Kativhu; Johnny Wang; James P Morken
Journal:  Angew Chem Int Ed Engl       Date:  2020-04-15       Impact factor: 15.336

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