Literature DB >> 25938383

Regiospecific Benzoylation of Electron-Deficient N-Heterocycles with Methylbenzenes via a Minisci-Type Reaction.

Wajid Ali1, Ahalya Behera1, Srimanta Guin1, Bhisma K Patel1.   

Abstract

A regioselective cross-dehydrogenative coupling between electron-deficient N-heterocycles (isoquinoline, quinolines, and quinoxalines) and methylbenzenes leading to regiospecific C-aroylation has been accomplished using AlCl3 as the catalyst in the presence of oxidant TBHP. This protocol is a practical alternative to the classical Minisci reaction.

Entities:  

Year:  2015        PMID: 25938383     DOI: 10.1021/acs.joc.5b00501

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  3 in total

1.  Photo-redox catalyzed dehydrazinative acylation of N-heterocycles via Minisci reaction.

Authors:  Saira Hafeez; Aamer Saeed
Journal:  RSC Adv       Date:  2021-12-01       Impact factor: 4.036

2.  Coordinating activation strategy for C(sp(3))-H/C(sp(3))-H cross-coupling to access β-aromatic α-amino acids.

Authors:  Kaizhi Li; Qian Wu; Jingbo Lan; Jingsong You
Journal:  Nat Commun       Date:  2015-09-29       Impact factor: 14.919

3.  Visible Light-Mediated Direct C-H Aroylation and Alkylation of Heteroarenes.

Authors:  Rui Chang; Jie Fang; Jian-Qiang Chen; Dan Liu; Guo-Qiang Xu; Peng-Fei Xu
Journal:  ACS Omega       Date:  2019-08-14
  3 in total

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