REACTIONS OF IMMONIUM AND TELLURONIUM SALTS OF 2-PHENYLBENZOTELLURAZOLE

Authors

  • Г. М. Абакаров Dagestan State Technical University, Makhachkala 367015
  • М.-З. В. Вагабов Dagestan State Technical University, Makhachkala 367015
  • В. А. Пантин Dagestan State Technical University, Makhachkala 367015
  • И. Д. Садеков Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don 344090
  • В. И. Минкин Institute of Physical and Organic Chemistry, Rostov State University, Rostov-on-Don 344090

DOI:

https://doi.org/10.1007/7431

Keywords:

N-methyl-2-phenylbenzotellurazolium iodide, 1-methyl-2-phenytelluronioazole perchlorate, reduction, hydrolysis, recyclization

Abstract

N-methyl-2-phenylbenzotellurazolinium iodide, like  other N-methylbenzochalcogenazolium salts, readily undergoes reduction, hydrolysis, and  recyclization  with hydrazine hydrate and  o-phenylene diamine. 1-Methyl-2-phenylbenzotelluronioazole perchlorate is  an effective methylating agent in reactions with nucleophiles.

How to Cite
Abakarov, G. M.; Vagabov, M.-Z. V.; Pantin, V. A.; Sadekov, I. D.; Minkin, V. I.  Chem. Heterocycl. Compd. 2007, 43, 1076. [Khim. Geterotsikl. Soedin. 2007, 1268.]

For this article in the English edition see DOI 10.1007/s10593-007-0168-9


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Published

2023-02-02

Issue

No. 8 (2007)

Section

Original Papers