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Mendeleev Communications, 2019, Volume 29, Issue 1, Pages 59–60
DOI: https://doi.org/10.1016/j.mencom.2019.01.019
(Mi mendc1421)
 

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

Communications

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

D. G. Kim, A. V. Rybakova, V. V. Sharutin, E. I. Danilina, O. V. Sazhayeva

South Ural State University (National Research University), Chelyabinsk, Russian Federation
Abstract: 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.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (350.8 Kb)


Citation: D. G. Kim, A. V. Rybakova, V. V. Sharutin, E. I. Danilina, O. V. Sazhayeva, “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”, Mendeleev Commun., 29:1 (2019), 59–60
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  • https://www.mathnet.ru/eng/mendc/v29/i1/p59
  • This publication is cited in the following 2 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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