Issue 6, 2002

Formation of an optically active 2-phenyl[1,2,4]triazolo[1,5-a]pyrimidine derivative in the reaction of (+)-3-carene-derived β-chlorovinylketone with benzylidene aminoguanidine

Abstract

The treatment of a seco-carane-type β-chlorovinyl ketone with benzylidene aminoguanidine in boiling methanol in the presence of sodium bicarbonate results in the formation of a substituted 2-phenyl[1,2,4]triazolo[1,5-a]pyrimidine.

Article information

Article type
Paper
Submitted
31 Oct 2002

Mendeleev Commun., 2002,12, 226-227

Formation of an optically active 2-phenyl[1,2,4]triazolo[1,5-a]pyrimidine derivative in the reaction of (+)-3-carene-derived β-chlorovinylketone with benzylidene aminoguanidine

S. A. Popov, T. V. Rybalova, Y. V. Gatilov and A. V. Tkachev, Mendeleev Commun., 2002, 12, 226 DOI: 10.1070/MC2002v012n06ABEH001678

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