Literature DB >> 28447094

α,β-Functionalization of saturated ketones with anthranils via Cu-catalyzed sequential dehydrogenation/aza-Michael addition/annulation cascade reactions in one-pot.

Dipak Kumar Tiwari1, Mandalaparthi Phanindrudu, Sandip Balasaheb Wakade, Jagadeesh Babu Nanubolu, Dharmendra Kumar Tiwari.   

Abstract

An efficient method to access functionalized quinolines from the readily available saturated ketones and anthranils has been explored. This one-pot cascade reaction involves the in situ generation of α,β-unsaturated ketones by the copper catalysed dehydrogenation of saturated ketones followed by the aza-Michael addition of anthranils and subsequent annulation.

Entities:  

Year:  2017        PMID: 28447094     DOI: 10.1039/c7cc01195d

Source DB:  PubMed          Journal:  Chem Commun (Camb)        ISSN: 1359-7345            Impact factor:   6.222


  2 in total

1.  An efficient 3-acylquinoline synthesis from acetophenones and anthranil via C(sp3)-H bond activation mediated by Selectfluor.

Authors:  Yejun Gao; Robert C Hider; Yongmin Ma
Journal:  RSC Adv       Date:  2019-04-02       Impact factor: 3.361

2.  Transition-metal-free approach to quinolines via direct oxidative cyclocondensation reaction of N,N-dimethyl enaminones with o-aminobenzyl alcohols.

Authors:  Kairui Rao; Zhangmengjie Chai; Pan Zhou; Donghan Liu; Yulin Sun; Fuchao Yu
Journal:  Front Chem       Date:  2022-09-21       Impact factor: 5.545

  2 in total

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