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

Journal Mendeleev Communications
ISSN: 0959-9436
Output data Year: 2002, Number: 6, Pages: 226-227 Pages count : DOI: 10.1070/MC2002v012n06ABEH001678
Authors Popov SA , Rybalova TV , Gatilov YV , Tkachev AV
Affiliations
1 (Данные Web of science) Novosibirsk State Univ, Dept Nat Sci, Novosibirsk 630090, Russia
2 (Данные Web of science) Russian Acad Sci, Siberian Branch, NN Vorozhtsov Novosibirsk Inst Organ Chem, Novosibirsk 630090, Russia

Abstract: The treatment of a seco-carane-type beta-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.
Cite: Popov S. , Rybalova T. , Gatilov Y. , Tkachev A.
Formation of an optically active 2-phenyl[1,2,4]triazolo[1,5-a]pyrimidine derivative in the reaction of (+)-3-carene-derived beta-chlorovinylketone with benzylidene aminoguanidine
Mendeleev Communications. 2002. N6. P.226-227. DOI: 10.1070/MC2002v012n06ABEH001678 WOS Scopus РИНЦ OpenAlex
Dates:
Published print: Jan 1, 2002
Identifiers:
Web of science: WOS:000181198500009
Scopus: 2-s2.0-0036881956
Elibrary: 13416092
OpenAlex: W2008688453
Citing:
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Web of science 2
Scopus 2
Elibrary 1
OpenAlex 2
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