Literature DB >> 22622200

A concise route to indoloazocines via a sequential Ugi-gold-catalyzed intramolecular hydroarylation.

Sachin G Modha1, Dipak D Vachhani, Jeroen Jacobs, Luc Van Meervelt, Erik V Van der Eycken.   

Abstract

A diversity oriented approach for the synthesis of indoloazocines is reported employing an Ugi reaction followed by a gold-catalyzed intramolecular hydroarylation.

Entities:  

Year:  2012        PMID： 22622200     DOI： 10.1039/c2cc32586a

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


  3 in total

1.  Gold(I)-Catalyzed Activation of Alkynes for the Construction of Molecular Complexity.

Authors:  Ruth Dorel; Antonio M Echavarren
Journal:  Chem Rev       Date:  2015-04-06       Impact factor: 60.622

2.  Post-Ugi gold-catalyzed diastereoselective domino cyclization for the synthesis of diversely substituted spiroindolines.

Authors:  Amit Kumar; Dipak D Vachhani; Sachin G Modha; Sunil K Sharma; Virinder S Parmar; Erik V Van der Eycken
Journal:  Beilstein J Org Chem       Date:  2013-10-14       Impact factor: 2.883

3.  A green protocol for the electrochemical synthesis of a fluorescent dye with antibacterial activity from imipramine oxidation.

Authors:  Zahra Souri; Mahmood Masoudi Khoram; Davood Nematollahi; Mohammad Mazloum-Ardakani; Hojjat Alizadeh
Journal:  Sci Rep       Date:  2022-03-22       Impact factor: 4.379
  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.