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Silver-catalysed intramolecular cyclisation of 2-alkynylacetophenones and 3-acetyl-2-alkynylpyridines in the presence of ammonia
Monica Dell'Acqua,Giorgio Abbiati,Antonio Arcadi,Elisabetta Rossi
Organic & Biomolecular Chemistry Pub Date : 08/16/2011 00:00:00 , DOI:10.1039/C1OB06271A
Abstract

Silver-catalysed/microwave-assisted domino reactions of 2-alkynyl-acetophenones and 3-acetyl-2-alkynylpyridines in the presence of ammonia are widely described. In most cases the reaction give a mixture of the imino- and carbo-cyclisation products, with a general preference for the former. A plausible mechanism is proposed and the dual activity of silver salts is supported by NMR experiments.

Graphical abstract: Silver-catalysed intramolecular cyclisation of 2-alkynylacetophenones and 3-acetyl-2-alkynylpyridines in the presence of ammonia
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