Literature DB >> 27992723

BF3·OEt2 Mediated Regioselective Reaction of Electron-Rich Arenes with 3-Ylidene Oxindoles.

Nitika Sharma1, Rama Krishna Peddinti1.   

Abstract

A BF3·OEt2 mediated novel and regioselective protocol for the construction of a C-C bond between 3-ylidene oxindoles and electron-rich arenes has been successfully accomplished. The reaction was compatible with a wide variety of electron-rich arenes. A cascade reaction of 3-ylidene oxindoles with phenols and β-naphthol resulted in 2,3-difunctionalized benzofuran and lactone bearing indoline-2-one scaffolds under same conditions.

Entities:  

Year:  2017        PMID: 27992723     DOI: 10.1021/acs.joc.6b02395

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


  2 in total

1.  Highly Regioselective Synthesis of Oxindolyl-Pyrroles and Quinolines via a One-Pot, Sequential Meyer-Schuster Rearrangement, Anti-Michael Addition/C(sp3)-H Functionalization, and Azacyclization.

Authors:  Srinivasarao Yaragorla; Ravikrishna Dada; P Rajesh; Manju Sharma
Journal:  ACS Omega       Date:  2018-03-09

2.  Improved Method for Preparation of 3-(1H-Indol-3-yl)benzofuran-2(3H)-ones.

Authors:  Igor Yu Grishin; Nikolai A Arutiunov; Dmitrii A Aksenov; Nicolai A Aksenov; Alexander V Aksenov; Amina Z Gasanova; Elena A Sorokina; Carolyn Lower; Michael Rubin
Journal:  Molecules       Date:  2022-03-15       Impact factor: 4.411

  2 in total

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