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Mendeleev Communications, 2002, Volume 12, Issue 6, Pages 226–227
DOI: https://doi.org/10.1070/MC2002v012n06ABEH001678
(Mi mendc4174)
 

This article is cited in 2 scientific papers (total in 2 papers)

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. Popova, T. V. Rybalovaa, Yu. V. Gatilova, A. V. Tkachevb

a N.N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, Siberian Branch of the Russian Academy of Sciences, Novosibirsk, Russian Federation
b Department of Natural Sciences, Novosibirsk State University, Novosibirsk, Russian Federation
Full-text PDF (105 kB) Citations (2)
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.
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Document Type: Article
Language: English


Citation: S. A. Popov, T. V. Rybalova, Yu. V. Gatilov, A. V. Tkachev, “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”, Mendeleev Commun., 12:6 (2002), 226–227
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  • https://www.mathnet.ru/eng/mendc/v12/i6/p226
  • This publication is cited in the following 2 articles:
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