Literature DB >> 12037558

Understanding and exploiting C-H bond activation.

Jay A Labinger1, John E Bercaw.   

Abstract

The selective transformation of ubiquitous but inert C H bonds to other functional groups has far-reaching practical implications, ranging from more efficient strategies for fine chemical synthesis to the replacement of current petrochemical feedstocks by less expensive and more readily available alkanes. The past twenty years have seen many examples of C-H bond activation at transition-metal centres, often under remarkably mild conditions and with high selectivity. Although profitable practical applications have not yet been developed, our understanding of how these organometallic reactions occur, and what their inherent advantages and limitations for practical alkane conversion are, has progressed considerably. In fact, the recent development of promising catalytic systems highlights the potential of organometallic chemistry for useful C-H bond activation strategies that will ultimately allow us to exploit Earth's alkane resources more efficiently and cleanly.

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Year:  2002        PMID: 12037558     DOI: 10.1038/417507a

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  188 in total

1.  Weak coordination as a powerful means for developing broadly useful C-H functionalization reactions.

Authors:  Keary M Engle; Tian-Sheng Mei; Masayuki Wasa; Jin-Quan Yu
Journal:  Acc Chem Res       Date:  2011-12-14       Impact factor: 22.384

2.  Ruthenium-catalyzed γ-carbolinium ion formation from aryl azides; synthesis of dimebolin.

Authors:  Huijun Dong; Regina T Latka; Tom G Driver
Journal:  Org Lett       Date:  2011-04-25       Impact factor: 6.005

3.  The key nickel enzyme of methanogenesis catalyses the anaerobic oxidation of methane.

Authors:  Silvan Scheller; Meike Goenrich; Reinhard Boecher; Rudolf K Thauer; Bernhard Jaun
Journal:  Nature       Date:  2010-06-03       Impact factor: 49.962

4.  Direct arylation of 6-phenylpurine and 6-arylpurine nucleosides by ruthenium-catalyzed C-H bond activation.

Authors:  Mahesh K Lakshman; Ashoke C Deb; Raghu Ram Chamala; Padmanava Pradhan; Ramendra Pratap
Journal:  Angew Chem Int Ed Engl       Date:  2011-09-28       Impact factor: 15.336

5.  Heterocycle Formation via Palladium-Catalyzed C-H Functionalization.

Authors:  Tian-Sheng Mei; Lei Kou; Sandy Ma; Keary M Engle; Jin-Quan Yu
Journal:  Synthesis (Stuttg)       Date:  2012-05-25       Impact factor: 3.157

6.  Directed evolution methods for overcoming trade-offs between protein activity and stability.

Authors:  Samuel D Stimple; Matthew D Smith; Peter M Tessier
Journal:  AIChE J       Date:  2019-10-09       Impact factor: 3.993

7.  Reactions of Anilines and Benzamides with a Fourteen-Electron Iridium(I) Bis(Phosphinite) Complex: N-H Oxidative Addition versus Lewis Base Coordination.

Authors:  Alison Cartwright Sykes; Peter White; Maurice Brookhart
Journal:  Organometallics       Date:  2006-03-27       Impact factor: 3.876

8.  Enzyme-mediated biodegradation of long-chain n-alkanes (C32 and C40) by thermophilic bacteria.

Authors:  Punniyakotti Elumalai; Punniyakotti Parthipan; Obulisamy Parthiba Karthikeyan; Aruliah Rajasekar
Journal:  3 Biotech       Date:  2017-05-31       Impact factor: 2.406

9.  Theoretical study on the activation of C-H bond in ethane by PdX+ (X = F, Cl, Br, H, and CH3) in the gas phase.

Authors:  Yu-Xiu Nie; Xiao-Xia Zhang; Yong-Ning Yuan; Feng Lu; Zhi-Yuan Geng
Journal:  J Mol Model       Date:  2020-04-03       Impact factor: 1.810

10.  Lessons from nature: unraveling biological CH bond activation.

Authors:  Kari L Stone; A S Borovik
Journal:  Curr Opin Chem Biol       Date:  2009-03-16       Impact factor: 8.822

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