Literature DB >> 22229784

SnCl2-catalyzed selective atom economic imino Diels-Alder reaction: synthesis of 2-(1H-pyrrolo[2,3-b]pyridin-3-yl)quinolines.

Rajendran Suresh1, Shanmugam Muthusubramanian, Rajendran Senthilkumaran, Govindaswamy Manickam.   

Abstract

The synthesis of 2-(1H-pyrrolo[2,3-b]pyridin-3-yl)quinolines by a SnCl(2)-catalyzed multicomponent reaction has been described. The reaction proceeds chemo- and regioselectively in an atom-economic way, generating a library of 24 quinoline derivatives.

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Year:  2012        PMID： 22229784     DOI： 10.1021/jo202256z

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


  3 in total

1.  An efficient and green synthesis of ferrocenyl-quinoline conjugates via a TsOH-catalyzed three-component reaction in water.

Authors:  Rui-Qi Mou; Mei Zhao; Xue-Xin Lv; Sheng-Yan Zhang; Dian-Shun Guo
Journal:  RSC Adv       Date:  2018-03-06       Impact factor: 4.036

2.  Spiro annulation of cage polycycles via Grignard reaction and ring-closing metathesis as key steps.

Authors:  Sambasivarao Kotha; Mohammad Saifuddin; Rashid Ali; Gaddamedi Sreevani
Journal:  Beilstein J Org Chem       Date:  2015-08-05       Impact factor: 2.883

3.  Catalytically active coordination polymer with a tiny Zn2Se2 ring bridged by bis-selone.

Authors:  Mannarsamy Maruthupandi; Ganesan Prabusankar
Journal:  RSC Adv       Date:  2020-08-04       Impact factor: 4.036
  3 in total

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