Literature DB >> 15307732

Regioselective formation of six- and seven-membered ring by intramolecular Pd-catalyzed amination of N-allyl-anthranilamides.

Egle M Beccalli1, Gianluigi Broggini, Giuseppe Paladino, Andrea Penoni, Caterina Zoni.   

Abstract

A divergent synthesis of quinazolin-4-ones and 1,4-benzodiazepin-5-ones by Pd(II)-catalyzed intramolecular amination of tosylated N-allyl-anthranilamides is described. Both kinds of products were available in high yields depending on the different reaction conditions. Copyright 2004 American Chemical Society

Entities:  

Year:  2004        PMID: 15307732     DOI: 10.1021/jo0495135

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


  5 in total

1.  Copper-promoted synthesis of 1,4-benzodiazepinones via alkene diamination.

Authors:  Shuklendu D Karyakarte; Fatima C Sequeira; Garrick H Zibreg; Guoqing Huang; Josiah P Matthew; Marina M M Ferreira; Sherry R Chemler
Journal:  Tetrahedron Lett       Date:  2015-06-03       Impact factor: 2.415

2.  Ir-Catalyzed Intermolecular Branch-Selective Allylic C-H Amidation of Unactivated Terminal Olefins.

Authors:  Honghui Lei; Tomislav Rovis
Journal:  J Am Chem Soc       Date:  2019-02-04       Impact factor: 15.419

3.  Aqueous hydrotrope: an efficient and reusable medium for a green one-pot, diversity-oriented synthesis of quinazolinone derivatives.

Authors:  Amol Patil; Madhuri Barge; Gajanan Rashinkar; Rajashri Salunkhe
Journal:  Mol Divers       Date:  2015-03-20       Impact factor: 2.943

4.  On the mechanism of nitrosoarene-alkyne cycloaddition.

Authors:  Andrea Penoni; Giovanni Palmisano; Yi-Lei Zhao; Kendall N Houk; Jerome Volkman; Kenneth M Nicholas
Journal:  J Am Chem Soc       Date:  2009-01-21       Impact factor: 15.419

5.  Copper-catalyzed oxidative amination and allylic amination of alkenes.

Authors:  Timothy W Liwosz; Sherry R Chemler
Journal:  Chemistry       Date:  2013-07-22       Impact factor: 5.236

  5 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.