Literature DB >> 35213165

Cu(II)-Catalyzed Synthesis of 4-(1,4,5,6-Tetrahydropyridin-3-yl)-1,4-dihydroisoquinolin-3-ones from 4-Diazoisoquinolin-3-ones.

Minghui Qi1, Muhammad Suleman1, Jianwei Xie1, Ping Lu1, Yanguang Wang1.   

Abstract

We report a simple, efficient, and highly selective C-H bond insertion of copper carbenes generated in situ from 4-diazo-1,4-dihydroisoquinolin-3-ones into β-C(sp2)-H bonds of N-sulfonyl enamides, which gave a series of 4-(1,4,5,6-tetrahydropyridin-3-yl)-1,4-dihydroisoquinolin-3(2H)-ones in good to excellent yields. Operationally simple and mild reaction conditions, a cheap catalyst, readily accessible starting materials, and a broad substrate scope are the merits of this reaction.

Entities:  

Year:  2022        PMID: 35213165     DOI: 10.1021/acs.joc.1c02905

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


  1 in total

1.  Facile and diastereoselective arylation of the privileged 1,4-dihydroisoquinolin-3(2H)-one scaffold.

Authors:  Dmitry Dar'in; Grigory Kantin; Alexander Bunev; Mikhail Krasavin
Journal:  Beilstein J Org Chem       Date:  2022-08-22       Impact factor: 2.544

  1 in total

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