Halo-heterocyclization of trans-5-phenyl-3-cinnamylsulfanyl[1,2,4]triazine into [1,3]thiazino[3,2-b][1,2,4]triazin-9-ium systems

Autor:	A. V. Rybakova, Elena I. Danilina, Vladimir V. Sharutin, Olesya V. Sazhayeva, Dmitry G. Kim
Rok vydání:	2019
Předmět:	Bromine 010405 organic chemistry chemistry.chemical_element General Chemistry 010402 general chemistry Iodine 01 natural sciences Medicinal chemistry 0104 chemical sciences chemistry.chemical_compound chemistry Thiazine Moiety Triazine Dichloromethane
Zdroj:	Mendeleev Communications. 29:59-60
ISSN:	0959-9436
DOI:	10.1016/j.mencom.2019.01.019
Popis:	Treatment of trans-5-phenyl-3-cinnamylsulfanyl[1,2,4]triazine with bromine or iodine in dichloromethane leads to haloannulation onto the thiazine moiety with formation of (7r,8t)-7-halo-3,8-diphenyl-7,8-dihydro-6H-[1,3]thiazino[3,2-b][1,2,4]-triazin-9-ium salts. The product structure was confirmed by X-ray study.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_________::09cae654f7f99281957aabf9765e7edb https://doi.org/10.1016/j.mencom.2019.01.019 Zobrazit plný text záznamu Full Text from ScienceDirect