Literature DB >> 24091429

Selection of boron reagents for Suzuki-Miyaura coupling.

Alastair J J Lennox1, Guy C Lloyd-Jones.   

Abstract

Suzuki-Miyaura (SM) cross-coupling is arguably the most widely-applied transition metal catalysed carbon-carbon bond forming reaction to date. Its success originates from a combination of exceptionally mild and functional group tolerant reaction conditions, with a relatively stable, readily prepared and generally environmentally benign organoboron reagent. A variety of such reagents have been developed for the process, with properties that have been tailored for application under specific SM coupling conditions. This review analyses the seven main classes of boron reagent that have been developed. The general physical and chemical properties of each class of reagent are evaluated with special emphasis on the currently understood mechanisms of transmetalation. The methods to prepare each reagent are outlined, followed by example applications in SM coupling.

Entities:  

Year:  2013        PMID: 24091429     DOI: 10.1039/c3cs60197h

Source DB:  PubMed          Journal:  Chem Soc Rev        ISSN: 0306-0012            Impact factor:   54.564


  108 in total

1.  A stepwise dechlorination/cross-coupling strategy to diversify the vancomycin 'in-chloride'.

Authors:  Tyler J Wadzinski; Katherine D Gea; Scott J Miller
Journal:  Bioorg Med Chem Lett       Date:  2015-12-11       Impact factor: 2.823

Review 2.  Merging Boron with Nitrogen-Oxygen Bonds: A Review on BON Heterocycles.

Authors:  Ivan S Golovanov; Alexey Yu Sukhorukov
Journal:  Top Curr Chem (Cham)       Date:  2021-02-05

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

Authors:  Andy A Thomas; Hao Wang; Andrew F Zahrt; Scott E Denmark
Journal:  J Am Chem Soc       Date:  2017-03-07       Impact factor: 15.419

4.  Chemical space screening around Phe3 in opioid peptides: Modulating µ versus δ agonism by Suzuki-Miyaura cross-couplings.

Authors:  Tom Willemse; Emilie Eiselt; Karlijn Hollanders; Wim Schepens; Herman W T van Vlijmen; Nga N Chung; Véronique Blais; Brain Holleran; Jean-Michel Longpré; Peter W Schiller; Bert U W Maes; Philippe Sarret; Louis Gendron; Steven Ballet
Journal:  Bioorg Med Chem Lett       Date:  2018-05-12       Impact factor: 2.823

5.  Enantioselective desymmetrization via carbonyl-directed catalytic asymmetric hydroboration and Suzuki-Miyaura cross-coupling.

Authors:  Gia L Hoang; Zhao-Di Yang; Sean M Smith; Rhitankar Pal; Judy L Miska; Damaris E Pérez; Libbie S W Pelter; Xiao Cheng Zeng; James M Takacs
Journal:  Org Lett       Date:  2015-02-02       Impact factor: 6.005

6.  Benzyltriboronates: Building Blocks for Diastereoselective Carbon-Carbon Bond Formation.

Authors:  W Neil Palmer; Cayetana Zarate; Paul J Chirik
Journal:  J Am Chem Soc       Date:  2017-02-13       Impact factor: 15.419

7.  A Functional Group Approach for Prediction of APPI Response of Organic Synthetic Targets.

Authors:  Konstantin O Zhurov; Laure Menin; Thomas Di Franco; Yury O Tsybin
Journal:  J Am Soc Mass Spectrom       Date:  2015-04-21       Impact factor: 3.109

8.  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

9.  A Dual Palladium and Copper Hydride Catalyzed Approach for Alkyl-Aryl Cross-Coupling of Aryl Halides and Olefins.

Authors:  Stig D Friis; Michael T Pirnot; Lauren N Dupuis; Stephen L Buchwald
Journal:  Angew Chem Int Ed Engl       Date:  2017-05-16       Impact factor: 15.336

10.  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

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