Literature DB >> 23134301

Intramolecular dehydrogenative coupling of sp2 C-H and sp3 C-H bonds: an expeditious route to 2-oxindoles.

Santanu Ghosh1, Subhadip De, Badrinath N Kakde, Subhajit Bhunia, Amit Adhikary, Alakesh Bisai.   

Abstract

An intramolecular-dehydrogenative-coupling (IDC) using "transition-metal-free" oxidation conditions has been achieved to synthesize a variety of 2-oxindoles bearing an all-carbon quaternary stereogenic center at the benzylic position. The methodology involves a one-pot C-alkylation of β-N-arylamido esters (3, 6) with alkyl halides using potassium tert-butoxide concomitant with a dehydrogenative coupling. A radical-mediated pathway has been tentatively proposed for the oxidative process.

Entities:  

Year:  2012        PMID: 23134301     DOI: 10.1021/ol302767w

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


  3 in total

1.  Synthesis of 2-oxindoles via 'transition-metal-free' intramolecular dehydrogenative coupling (IDC) of sp(2) C-H and sp(3) C-H bonds.

Authors:  Nivesh Kumar; Santanu Ghosh; Subhajit Bhunia; Alakesh Bisai
Journal:  Beilstein J Org Chem       Date:  2016-06-08       Impact factor: 2.883

2.  Oxindole synthesis via polar-radical crossover of ketene-derived amide enolates in a formal [3 + 2] cycloaddition.

Authors:  Niklas Radhoff; Armido Studer
Journal:  Chem Sci       Date:  2022-03-09       Impact factor: 9.825

3.  Green oxidation of indoles using halide catalysis.

Authors:  Jun Xu; Lixin Liang; Haohao Zheng; Yonggui Robin Chi; Rongbiao Tong
Journal:  Nat Commun       Date:  2019-10-18       Impact factor: 14.919

  3 in total

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