Indolopyridines containing a bridgehead heteroatom 12. Synthesis and reduction of 12-arylidene-5,6-dihydroindolo[2,1-a]isoquinolinium trifluoroacetates

Condensation of 5,6-dihydroindolo[2,1-a]isoquinoline with aromatic aldehydes in trifluoroacetic acid afforded 12-arylidene-5,6-dihydroindolo[2,1-a]isoquinolinium trifluoroacetates. Hydrogenolysis of these salts on rhenium heptasulfide at elevated temperature and hydrogen pressure yielded indolo [2,1-a]isoquinolines, while reduction with sodium borohydride gave 12-arylmethylindoloisoquinolines. Photoluminescence was found for some indolo[2,1-a]isoquinolines.

Авторы
Номер выпуска
11
Язык
Английский
Страницы
2116-2120
Статус
Опубликовано
Том
51
Год
2002
Организации
  • 1 Peoples Friendship University, 3 ul. Ordzhonikidze, 117198 Moscow, Russian Federation
  • 2 N. D. Zelinsky Inst. of Organ. Chem., Russian Academy of Sciences, 47 Leninsky prosp., 119991 Moscow, Russian Federation
Ключевые слова
12-arylidene-5,6-dihydroindolo[2,1-a]isoquinolinium trifuoroacetates; 12-benzylindolo[2,1-a]isoquinolines; 5,6-dihydroindolo[2,1-a]isoquinolines; Hydrogenolysis; Photoluminescent properties; Reduction; Rhenium heptasulfide; Sodium borohydride
Цитировать
Поделиться

Другие записи

Sokol V.I., Yakimenko O.A., Davydov V.V., Shklyaev Yu.V., Sergienko V.S., Ryabov M.A.
Химия гетероциклических соединений. Латвийский институт органического синтеза Латвийской академии наук / Springer New York Consultants Bureau. Том 38. 2002. С. 1497-1503