Literature DB >> 21898724

Synthesis and reactions of N-heterocyclic carbene boranes.

Dennis P Curran1, Andrey Solovyev, Malika Makhlouf Brahmi, Louis Fensterbank, Max Malacria, Emmanuel Lacôte.   

Abstract

Boranes are widely used Lewis acids and N-heterocyclic carbenes (NHCs) are popular Lewis bases, so it is remarkable how little was known about their derived complexes until recently. NHC-boranes are typically readily accessible and many are so stable that they can be treated like organic compounds rather than complexes. They do not exhibit "borane chemistry", but instead are proving to have a rich chemistry of their own as reactants, as reagents, as initiators, and as catalysts. They have significant potential for use in organic synthesis and in polymer chemistry. They can be used to easily make unusual complexes with a broad spectrum of functional groups not usually seen in organoboron chemistry. Many of their reactions occur through new classes of reactive intermediates including borenium cations, boryl radicals, and even boryl anions. This Review provides comprehensive coverage of the synthesis, characterization, and reactions of NHC-boranes.
Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Year:  2011        PMID: 21898724     DOI: 10.1002/anie.201102717

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  33 in total

1.  Genetically programmed chiral organoborane synthesis.

Authors:  S B Jennifer Kan; Xiongyi Huang; Yosephine Gumulya; Kai Chen; Frances H Arnold
Journal:  Nature       Date:  2017-11-29       Impact factor: 49.962

2.  Metal-free catalytic enantioselective C-B bond formation: (pinacolato)boron conjugate additions to α,β-unsaturated ketones, esters, Weinreb amides, and aldehydes promoted by chiral N-heterocyclic carbenes.

Authors:  Hao Wu; Suttipol Radomkit; Jeannette M O'Brien; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2012-05-04       Impact factor: 15.419

3.  Borenium ion catalyzed hydroboration of alkenes with N-heterocyclic carbene-boranes.

Authors:  Aleksandrs Prokofjevs; Anne Boussonnière; Linfeng Li; Hélène Bonin; Emmanuel Lacôte; Dennis P Curran; Edwin Vedejs
Journal:  J Am Chem Soc       Date:  2012-07-16       Impact factor: 15.419

4.  An overview of N-heterocyclic carbenes.

Authors:  Matthew N Hopkinson; Christian Richter; Michael Schedler; Frank Glorius
Journal:  Nature       Date:  2014-06-26       Impact factor: 49.962

5.  Synthesis and minisci reactions of organotrifluoroborato building blocks.

Authors:  Marc Presset; Nicolas Fleury-Brégeot; Daniel Oehlrich; Frederik Rombouts; Gary A Molander
Journal:  J Org Chem       Date:  2013-04-17       Impact factor: 4.354

6.  Carbene-Stabilized Main Group Radicals and Radical Ions.

Authors:  Caleb D Martin; Michele Soleilhavoup; Guy Bertrand
Journal:  Chem Sci       Date:  2013-08-01       Impact factor: 9.825

7.  Deprotonation of a borohydride: synthesis of a carbene-stabilized boryl anion.

Authors:  David A Ruiz; Gaël Ung; Mohand Melaimi; Guy Bertrand
Journal:  Angew Chem Int Ed Engl       Date:  2013-06-13       Impact factor: 15.336

8.  Mechanism of NHC-Catalyzed Conjugate Additions of Diboron and Borosilane Reagents to α,β-Unsaturated Carbonyl Compounds.

Authors:  Hao Wu; Jeannette M Garcia; Fredrik Haeffner; Suttipol Radomkit; Adil R Zhugralin; Amir H Hoveyda
Journal:  J Am Chem Soc       Date:  2015-08-11       Impact factor: 15.419

9.  Changes in ligating abilities of the singlet and triplet states of normal, abnormal and remote N-heterocyclic carbenes depending on their aromaticities.

Authors:  Resul Sevinçek; Hande Karabıyık; Hasan Karabıyık
Journal:  J Mol Model       Date:  2013-10-25       Impact factor: 1.810

10.  Flow Giese reaction using cyanoborohydride as a radical mediator.

Authors:  Takahide Fukuyama; Takuji Kawamoto; Mikako Kobayashi; Ilhyong Ryu
Journal:  Beilstein J Org Chem       Date:  2013-09-03       Impact factor: 2.883

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