Reaction of indolizines with elemental sulfur

The fusion of 3,8-diphenyl-, 1,2-diphenyl-, and 6-methyl-2,7-diphenyl-indolizines with sulfur results in the formation of bis(indolizin-3-yl) disulfides with the respective substituents. Bis(2,8-diphenylindolizin-3-yl) disulfide is reduced to the original indolizine, and its treatment with nitric acid gives 2,8-diphenyl-1, 3-dinitroindolizine. Bis(dibenzo[b,g]indolizin-11-yl) disulfide is obtained from dibenzo[b,g]indolizine. The formation of the disulfides is apparently a general region of indolizines without substituents at C3 or C1 of the pyrrole ring. The structures of the disulfides obtained have been confirmed by data from x-ray diffraction analysis and NMR spectroscopy. © 1985 Plenum Publishing Corporation.

Редакторы
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Издательство
Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau
Номер выпуска
10
Язык
Английский
Страницы
1128-1132
Статус
Опубликовано
Подразделение
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Номер
-
Том
20
Год
1984
Организации
  • 1 Patrice Lumumba Peoples' Friendship University, Moscow, 117923, Russian Federation
Ключевые слова
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Дата создания
19.10.2018
Дата изменения
19.10.2018
Постоянная ссылка
https://repository.rudn.ru/ru/records/article/record/1380/