Rearrangement of 2-iminoperhydrothieno-[3,4-<i>d</i>]thiazole 5,5-dioxides

Authors

  • А. Г. Макаренко Institute of Bioorganic Chemistry and Petroleum Chemistry, National Academy of Sciences of Ukraine, 253660, Kiev
  • П. И. Пархоменко Institute of Bioorganic Chemistry and Petroleum Chemistry, National Academy of Sciences of Ukraine, 253660, Kiev
  • А. Б. Роженко Institute of Bioorganic Chemistry and Petroleum Chemistry, National Academy of Sciences of Ukraine, 253660, Kiev
  • А. А. Григорьев Institute of Bioorganic Chemistry and Petroleum Chemistry, National Academy of Sciences of Ukraine, 253660, Kiev
  • М. В. Рыбакова Institute of Bioorganic Chemistry and Petroleum Chemistry, National Academy of Sciences of Ukraine, 253660, Kiev
  • Ю. В. Безуглый Institute of Bioorganic Chemistry and Petroleum Chemistry, National Academy of Sciences of Ukraine, 253660, Kiev

Abstract

The reaction of 4-bromo-2-thiolene 1,1-dioxide with thiosemicarbazide and thiosemicarbazones gave 2-iminoperhydrothieno[3,4-d]thiazole 5,5-dioxides, which contain a nitrogen function at the imino group. The recyclization of these compounds was studied.

How to Cite
Makarenko, A. G.; Parkhomenko, P. I.; Rozhenko, A. B.; Grigor'ev, A. A.; Rybakova, M. V.; Bezuglyi, Yu. V. Chem. Heterocycl. Compd. 1994, 30, 1106. [Khim. Geterotsikl. Soedin. 1994, 1274.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01171175

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Published

1994-09-25

Issue

No. 9 (1994)

Section

Original Papers