Electrophilically activated nitroalkanes in the synthesis of 6,7-dihydro-1H-cyclopenta[g]perimidines

A highly efficient synthetic route to 6,7-dihydro-1H-cyclopenta[gh]perimidines has been proposed on the basis of a novel reaction of nitroalkanes with 4,5-diaminoacenaphthene in the presence of polyphosphoric acid. The reaction involves phosphorylation of the aci-nitro compound, followed by intramolecular cyclization. © 2017, Pleiades Publishing, Ltd.

Авторы
Aksenov A.V. 1 , Aksenov N.A. 2, 1 , Ovcharov D.S. 1 , Shcherbakov S.V. 1 , Smirnova A.N. 1 , Aksenova I.V. 1 , Goncharov V.I. 1 , Rubin M.A. 1, 3
Номер выпуска
7
Язык
Английский
Страницы
1081-1084
Статус
Опубликовано
Том
53
Год
2017
Организации
  • 1 North-Caucasus Federal University, ul. Pushkina 1a, Stavropol, 355009, Russian Federation
  • 2 Peoples’ Friendship University of Russia, ul Miklukho-Maklaya 6, Moscow, 117198, Russian Federation
  • 3 University of Kansas, 1251 Wescoe Hall Drive, Lawrence, KS 66045, United States
Цитировать
Поделиться

Другие записи