Literature DB >> 12537484

Selective, catalytic carbon-carbon bond activation and functionalization promoted by late transition metal catalysts.

Suzanne C Bart1, Paul J Chirik.   

Abstract

The selective catalytic activation and functionalization of carbon-carbon bonds in a series of substituted cyclopropane substrates has been developed using commercially available transition metal catalysts. Catalytic hydrogenation and olefination procedures, tolerant of a range of functional groups, have been discovered. Introduction of a chelate-assisting substituent such as [PPh2] is effective in altering the kinetic selectivity and lowering the activation barrier for the catalytic processes.

Entities:  

Year:  2003        PMID: 12537484     DOI: 10.1021/ja028912j

Source DB:  PubMed          Journal:  J Am Chem Soc        ISSN: 0002-7863            Impact factor:   15.419


  5 in total

1.  Synthesis of α-Arylphosphonates Using Copper-Catalyzed α-Arylation and Deacylative α-Arylation of β-Ketophosphonates.

Authors:  Laxmidhar Rout; Sridhar Regati; Cong-Gui Zhao
Journal:  Adv Synth Catal       Date:  2011-12-06       Impact factor: 5.837

2.  Carbonylative N-Heterocyclization via Nitrogen-Directed C-C Bond Activation of Nonactivated Cyclopropanes.

Authors:  Adam D J Calow; David Dailler; John F Bower
Journal:  J Am Chem Soc       Date:  2022-06-17       Impact factor: 16.383

3.  Synthesis and applications of rhodacyclopentanones derived from C-C bond activation.

Authors:  Megan H Shaw; John F Bower
Journal:  Chem Commun (Camb)       Date:  2016-07-07       Impact factor: 6.222

4.  Rh-catalyzed regiodivergent hydrosilylation of acyl aminocyclopropanes controlled by monophosphine ligands.

Authors:  Hiroki Kondo; Kenichiro Itami; Junichiro Yamaguchi
Journal:  Chem Sci       Date:  2017-03-15       Impact factor: 9.825

5.  Ring-opening hydroarylation of monosubstituted cyclopropanes enabled by hexafluoroisopropanol.

Authors:  Edward Richmond; Jing Yi; Vuk D Vuković; Fatima Sajadi; Christopher N Rowley; Joseph Moran
Journal:  Chem Sci       Date:  2018-06-28       Impact factor: 9.825

  5 in total

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