Literature DB >> 20820665

A domino synthesis of benzoquinolinamide in the presence of iodine.

Li-Yan Zeng1, Chun Cai.   

Abstract

The domino synthesis of benzo[f]quinolinyl and benzo[h]quinolinyl acetamides from diketene, amines, aromatic aldehydes and naphthalenamine was developed, and the catalyst iodine was found to be crucial to the reaction. The structure was deduced from the mass spectrum, (1)H NMR, (13)C NMR spectrum and 2D NMR performed on two representative products.

Entities:  

Year:  2010        PMID: 20820665     DOI: 10.1039/c0ob00364f

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Synthesis of novel isoquinolinone and 1,2-dihydroisoquinoline scaffolds via Ugi reaction and ring opening reaction of furans.

Authors:  Fei Ji; Wen-bin Yi; Mu Sun; Mei-fang Lv; Chun Cai
Journal:  Mol Divers       Date:  2013-03-20       Impact factor: 2.943

  1 in total

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