Literature DB >> 22913435

Construction of nitrogen-fused tetrahydroquinolines via a domino reaction.

Nicolas Gigant1, Isabelle Gillaizeau.   

Abstract

An efficient domino approach for the diastereoselective synthesis of polyfunctionalized nitrogen-fused tetrahydroquinoline frameworks under mild conditions has been developed. The scope and limitation of this transformation were investigated by using a range of readily accessible enamides and benzyl azides. This method is also applicable to the formation of 2,3-functionalized enamides.

Entities:  

Year:  2012        PMID: 22913435     DOI: 10.1021/ol3020732

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


  2 in total

1.  Micro-flow nanocatalysis: synergic effect of TfOH@SPIONs and micro-flow technology as an efficient and robust catalytic system for the synthesis of plasticizers.

Authors:  Maryam Tashi; Behnaz Shafiee; Yoshie Sakamaki; Ji-Yun Hu; Zachary Heidrick; Ahmad R Khosropour; M Hassan Beyzavi
Journal:  RSC Adv       Date:  2018-11-13       Impact factor: 3.361

Review 2.  Recent syntheses of 1,2,3,4-tetrahydroquinolines, 2,3-dihydro-4(1H)-quinolinones and 4(1H)-quinolinones using domino reactions.

Authors:  Baskar Nammalwar; Richard A Bunce
Journal:  Molecules       Date:  2013-12-24       Impact factor: 4.411

  2 in total

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