Literature DB >> 11719693

Remarkably selective iridium catalysts for the elaboration of aromatic C-H bonds.

Jian-Yang Cho1, Man Kin Tse, Daniel Holmes, Robert E Maleczka, Milton R Smith.   

Abstract

Arylboron compounds have intriguing properties and are important building blocks for chemical synthesis. A family of Ir catalysts now enables the direct synthesis of arylboron compounds from aromatic hydrocarbons and boranes under "solventless" conditions. The Ir catalysts are highly selective for C-H activation and do not interfere with subsequent in situ transformations, including Pd-mediated cross-couplings with aryl halides. By virtue of their favorable activities and exceptional selectivities, these Ir catalysts impart the synthetic versatility of arylboron reagents to C-H bonds in aromatic and heteroaromatic hydrocarbons.

Entities:  

Mesh:

Substances:

Year:  2001        PMID: 11719693     DOI: 10.1126/science.1067074

Source DB:  PubMed          Journal:  Science        ISSN: 0036-8075            Impact factor:   47.728


  119 in total

Review 1.  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

2.  Unsupported boron-carbon σ-coordination to platinum as an isolable snapshot of σ-bond activation.

Authors:  Holger Braunschweig; Peter Brenner; Rian D Dewhurst; Ivo Krummenacher; Bernd Pfaffinger; Alfredo Vargas
Journal:  Nat Commun       Date:  2012-05-29       Impact factor: 14.919

3.  Palladium-catalyzed borylation of primary alkyl bromides.

Authors:  Amruta Joshi-Pangu; Xinghua Ma; Mohamed Diane; Sidra Iqbal; Robert J Kribs; Richard Huang; Chao-Yuan Wang; Mark R Biscoe
Journal:  J Org Chem       Date:  2012-07-23       Impact factor: 4.354

4.  PyDipSi: a general and easily modifiable/traceless Si-tethered directing group for C-H acyloxylation of arenes.

Authors:  Natalia Chernyak; Alexander S Dudnik; Chunhui Huang; Vladimir Gevorgyan
Journal:  J Am Chem Soc       Date:  2010-06-23       Impact factor: 15.419

5.  C-H activation: Following directions.

Authors:  Lutz Ackermann; Jie Li
Journal:  Nat Chem       Date:  2015-09       Impact factor: 24.427

6.  A meta-selective C-H borylation directed by a secondary interaction between ligand and substrate.

Authors:  Yoichiro Kuninobu; Haruka Ida; Mitsumi Nishi; Motomu Kanai
Journal:  Nat Chem       Date:  2015-08-17       Impact factor: 24.427

7.  Ligand-Enabled Meta-C-H Alkylation and Arylation Using a Modified Norbornene.

Authors:  Peng-Xiang Shen; Xiao-Chen Wang; Peng Wang; Ru-Yi Zhu; Jin-Quan Yu
Journal:  J Am Chem Soc       Date:  2015-09-03       Impact factor: 15.419

8.  meta-C-H Arylation and Alkylation of Benzylsulfonamide Enabled by a Palladium(II)/Isoquinoline Catalyst.

Authors:  Guolin Cheng; Peng Wang; Jin-Quan Yu
Journal:  Angew Chem Int Ed Engl       Date:  2017-06-09       Impact factor: 15.336

9.  Meta-selective C-H functionalization using a nitrile-based directing group and cleavable Si-tether.

Authors:  Sunggi Lee; Hyelee Lee; Kian L Tan
Journal:  J Am Chem Soc       Date:  2013-12-10       Impact factor: 15.419

10.  Activation of sp3 C-H bonds with cobalt(I): catalytic synthesis of enamines.

Authors:  Andrew D Bolig; Maurice Brookhart
Journal:  J Am Chem Soc       Date:  2007-11-07       Impact factor: 15.419

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.