Literature DB >> 19750753

N-heterocyclic carbenes: a new concept in organometallic catalysis.

Wolfgang A Herrmann1.   

Abstract

N-Heterocyclic carbenes have become universal ligands in organometallic and inorganic coordination chemistry. They not only bind to any transition metal, be it in low or high oxidation states, but also to main group elements such as beryllium, sulfur, and iodine. Because of their specific coordination chemistry, N-heterocyclic carbenes both stabilize and activate metal centers in quite different key catalytic steps of organic syntheses, for example, C-H activation, C-C, C-H, C-O, and C-N bond formation. There is now ample evidence that in the new generation of organometallic catalysts the established ligand class of organophosphanes will be supplemented and, in part, replaced by N-heterocyclic carbenes. Over the past few years, this chemistry has been the field of vivid scientific competition, and yielded previously unexpected successes in key areas of homogeneous catalysis. From the work in numerous academic laboratories and in industry, a revolutionary turning point in oraganometallic catalysis is emerging.

Entities:  

Year:  2002        PMID: 19750753     DOI: 10.1002/1521-3773(20020415)41:8<1290::aid-anie1290>3.0.co;2-y

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


  169 in total

1.  Structurally Characterized Cationic Silver(I) and Ruthenium(II)carbene complexes of 1,2,3-Triazol-5-ylidenes.

Authors:  Jiajia Cai; Xiaoping Yang; Kuppuswamy Arumugam; Christopher W Bielawski; Jonathan L Sessler
Journal:  Organometallics       Date:  2011-09-26       Impact factor: 3.876

2.  CO fixation to stable acyclic and cyclic alkyl amino carbenes: stable amino ketenes with a small HOMO-LUMO gap.

Authors:  Vincent Lavallo; Yves Canac; Bruno Donnadieu; Wolfgang W Schoeller; Guy Bertrand
Journal:  Angew Chem Int Ed Engl       Date:  2006-05-19       Impact factor: 15.336

Review 3.  Nickel-catalyzed cross-couplings involving carbon-oxygen bonds.

Authors:  Brad M Rosen; Kyle W Quasdorf; Daniella A Wilson; Na Zhang; Ana-Maria Resmerita; Neil K Garg; Virgil Percec
Journal:  Chem Rev       Date:  2010-12-06       Impact factor: 60.622

4.  Reaction of carbon dioxide with a palladium-alkyl complex supported by a bis-NHC framework.

Authors:  Piyal W G Ariyananda; Glenn P A Yap; Joel Rosenthal
Journal:  Dalton Trans       Date:  2012-05-30       Impact factor: 4.390

5.  A rigid cyclic (alkyl)(amino)carbene ligand leads to isolation of low-coordinate transition-metal complexes.

Authors:  Vincent Lavallo; Yves Canac; Alan DeHope; Bruno Donnadieu; Guy Bertrand
Journal:  Angew Chem Int Ed Engl       Date:  2005-11-11       Impact factor: 15.336

6.  An efficient synthesis of achiral and chiral 1,2,4-triazolium salts: bench stable precursors for N-heterocyclic carbenes.

Authors:  Mark S Kerr; Javier Read de Alaniz; Tomislav Rovis
Journal:  J Org Chem       Date:  2005-07-08       Impact factor: 4.354

7.  Stable cyclic (alkyl)(amino)carbenes as rigid or flexible, bulky, electron-rich ligands for transition-metal catalysts: a quaternary carbon atom makes the difference.

Authors:  Vincent Lavallo; Yves Canac; Carsten Präsang; Bruno Donnadieu; Guy Bertrand
Journal:  Angew Chem Int Ed Engl       Date:  2005-09-05       Impact factor: 15.336

Review 8.  Flexible design of ionic liquids for membrane interactions.

Authors:  Lena Rakers; Frank Glorius
Journal:  Biophys Rev       Date:  2018-03-16

9.  Synthesis and isolation of a stable, axially-chiral seven-membered N-heterocyclic carbene.

Authors:  Christopher C Scarborough; Ilia A Guzei; Shannon S Stahl
Journal:  Dalton Trans       Date:  2009-02-13       Impact factor: 4.390

10.  Asymmetric intermolecular boron Heck-type reactions via oxidative palladium(II) catalysis with chiral tridentate NHC-amidate-alkoxide ligands.

Authors:  Kyung Soo Yoo; Justin O'Neill; Satoshi Sakaguchi; Richard Giles; Joo Ho Lee; Kyung Woon Jung
Journal:  J Org Chem       Date:  2010-01-01       Impact factor: 4.354

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