Literature DB >> 19610606

Efficient synthesis of the indoloazocine framework via intramolecular alkyne carbocyclization.

Pavel A Donets1, Kristof Van Hecke, Luc Van Meervelt, Erik V Van der Eycken.   

Abstract

A microwave-assisted protocol based on an Hg(OTf)(2) catalyzed intramolecular alkyne carbocyclization reaction was developed for selective construction of the indoloazocine core.

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Year:  2009        PMID： 19610606     DOI： 10.1021/ol901356h

Source DB:  PubMed          Journal:  Org Lett        ISSN： 1523-7052            Impact factor:   6.005


  4 in total

Review 1.  Comprehensive survey of chemical libraries for drug discovery and chemical biology: 2009.

Authors:  Roland E Dolle; Bertrand Le Bourdonnec; Karin Worm; Guillermo A Morales; Craig J Thomas; Wei Zhang
Journal:  J Comb Chem       Date:  2010-10-05

2.  Novel approach to the lundurine alkaloids: synthesis of the tetracyclic core.

Authors:  Suvi T M Orr; Jianhua Tian; Meike Niggemann; Stephen F Martin
Journal:  Org Lett       Date:  2011-09-02       Impact factor: 6.005

3.  Synthetic studies toward lapidilectine-type Kopsia alkaloids.

Authors:  Erica E Schultz; Brian G Pujanauski; Richmond Sarpong
Journal:  Org Lett       Date:  2012-01-03       Impact factor: 6.005

4.  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
  4 in total

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