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 |
|
||||
Affiliations |
|
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
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
Dates:
Published print: | Jan 1, 2002 |
Identifiers:
Web of science | WOS:000181198500009 |
Scopus | 2-s2.0-0036881956 |
Elibrary | 13416092 |
OpenAlex | W2008688453 |