Literature DB >> 20000736

Gold-catalyzed cyclization of alkynylaziridines as an efficient approach toward functionalized N-phth pyrroles.

Xiangwei Du1, Xin Xie, Yuanhong Liu.   

Abstract

An efficient access to N-phth pyrrroles via gold-catalyzed cycloisomerization of N-phth alkynylaziridines has been described. Functionalized pyrroles including pyrrole-2-carboxylates or 2-pyrrolyl ketone are easily constructed in generally good yields by this method. The resulting pyrroles can be further converted to N-amino pyrrole or 2-acyl pyrrole, which are important synthetic intermediates for amplification of molecular complexity.

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Year:  2010        PMID: 20000736     DOI: 10.1021/jo902357x

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


  3 in total

Review 1.  Transition metal-mediated synthesis of monocyclic aromatic heterocycles.

Authors:  Anton V Gulevich; Alexander S Dudnik; Natalia Chernyak; Vladimir Gevorgyan
Journal:  Chem Rev       Date:  2013-01-10       Impact factor: 60.622

2.  Isotopic labelling studies for a gold-catalysed skeletal rearrangement of alkynyl aziridines.

Authors:  Paul W Davies; Nicolas Martin; Neil Spencer
Journal:  Beilstein J Org Chem       Date:  2011-06-21       Impact factor: 2.883

3.  Recent advances in the gold-catalyzed additions to C-C multiple bonds.

Authors:  He Huang; Yu Zhou; Hong Liu
Journal:  Beilstein J Org Chem       Date:  2011-07-04       Impact factor: 2.883

  3 in total

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