Literature DB >> 32645265

Highly Selective and Divergent Acyl and Aryl Cross-Couplings of Amides via Ir-Catalyzed C-H Borylation/N-C(O) Activation.

Pengcheng Gao1, Michal Szostak1.   

Abstract

Herein, we demonstrate that amides can be readily coupled with nonactivated arenes via sequential Ir-catalyzed C-H borylation/N-C(O) activation. This methodology provides facile access to biaryl ketones and biaryls by the sterically controlled Ir-catalyzed C-H borylation and divergent acyl and decarbonylative amide N-C(O) and C-C activation. The methodology diverts the traditional acylation and arylation regioselectivity, allowing us to directly utilize readily available arenes and amides to produce valuable ketone and biaryl motifs.

Entities:  

Year:  2020        PMID: 32645265     DOI: 10.1021/acs.orglett.0c02105

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  2 in total

1.  Decarbonylative Pd-Catalyzed Suzuki Cross-Coupling for the Synthesis of Structurally Diverse Heterobiaryls.

Authors:  Alejandro Cervantes-Reyes; Aaron C Smith; Gary M Chinigo; David C Blakemore; Michal Szostak
Journal:  Org Lett       Date:  2022-02-24       Impact factor: 6.072

2.  Fe(iii)-catalysed selective C-N bond cleavage of N-phenylamides by an electrochemical method.

Authors:  Yiwen Xu; Yang Long; Runyou Ye; Qiang Li; Fang Ke; Xiangge Zhou
Journal:  RSC Adv       Date:  2022-08-25       Impact factor: 4.036

  2 in total

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