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.

Authors
Aksenov A.V.1 , Aksenov N.A. 1, 2 , 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
Number of issue
7
Language
English
Pages
1081-1084
Status
Published
Volume
53
Year
2017
Organizations
  • 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
Date of creation
19.10.2018
Date of change
19.10.2018
Short link
https://repository.rudn.ru/en/records/article/record/5445/
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