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Synthesis of 7-oxindolylidene-3a,9a-diphenylimidazothiazolo[2,3-c][1,2,4]triazines by skeletal rearrangement of their [3,2-b]-fused isomers Full article

Journal Mendeleev Communications
ISSN: 1364-551X , E-ISSN: 0959-9436
Output data Year: 2022, Volume: 32, Number: 5, Pages: 678-679 Pages count : 2 DOI: 10.1016/j.mencom.2022.09.037
Authors Izmest'ev Alexei N. 1 , Kravchenko Angelina N. 1 , Gazieva Galina A. 1
Affiliations
1 N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, 119991 Moscow, Russian Federation

Abstract: Previously unavailable 7-oxindolylidene-1,3-dimethyl-3a,9adiphenylimidazo[4,5-e]thiazolo[2,3-c][1,2,4]triazines were obtained in 63–90% yields by skeletal amidine rearrangement of the thiazolo-triazine system in the corresponding imidazo[4,5-e]thiazolo[3,2-b][1,2,4]triazines on treatment with sodium methoxide.
Cite: Izmest'ev A.N. , Kravchenko A.N. , Gazieva G.A.
Synthesis of 7-oxindolylidene-3a,9a-diphenylimidazothiazolo[2,3-c][1,2,4]triazines by skeletal rearrangement of their [3,2-b]-fused isomers
Mendeleev Communications. 2022. V.32. N5. P.678-679. DOI: 10.1016/j.mencom.2022.09.037 WOS Scopus OpenAlex
Identifiers:
≡ Web of science: WOS:000874166100037
≡ Scopus: 2-s2.0-85139364793
≡ OpenAlex: W4302759588
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