Phosphorylation of Benzimidazole-2-thiones by Chloroethynylphosphonate


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The reaction of chloroethynylphosphonates with N-substituted benzimidazole-2-thiones proceeded chemo- and regioselectively with the formation of cyclic zwitterions, namely alkyl (9H-benzo[4,5]imidazo[2,1-b]-thiazol-3-yl-4-ium)phosphonates. Chemo- and regioselective reaction of N-unsubstituted benzimidazole-2-thione with chloroethynylphosphonates led to the production of linear Z-1,2-bis(1H-benzimidazol-2-ylsulfanyl)-ethenylphosphonates.

作者简介

D. Egorov

St. Petersburg State Institute of Technology (Technical University)

Email: dog_alla@mail.ru
俄罗斯联邦, Moskovskii pr. 26, St. Petersburg, 190013

Yu. Piterskaya

St. Petersburg State Institute of Technology (Technical University)

Email: dog_alla@mail.ru
俄罗斯联邦, Moskovskii pr. 26, St. Petersburg, 190013

D. Kartsev

St. Petersburg State Institute of Technology (Technical University)

Email: dog_alla@mail.ru
俄罗斯联邦, Moskovskii pr. 26, St. Petersburg, 190013

V. Polukeev

Institute of Experimental Medicine

Email: dog_alla@mail.ru
俄罗斯联邦, St. Petersburg

M. Krivchun

St. Petersburg State Institute of Technology (Technical University)

Email: dog_alla@mail.ru
俄罗斯联邦, Moskovskii pr. 26, St. Petersburg, 190013

A. Dogadina

St. Petersburg State Institute of Technology (Technical University)

编辑信件的主要联系方式.
Email: dog_alla@mail.ru
俄罗斯联邦, Moskovskii pr. 26, St. Petersburg, 190013

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