Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/14300
Title: Novel synthetic approach to pyrrolo[1,2-b]cinnolines
Authors: Demidov, O. P.
Демидов, О. П.
Aksenov, N. A.
Аксенов, Н. А.
Keywords: Aza-heterocycles;Cinnolines;Furan ring opening;Pyrrolo[1,2-b]cinnolines
Issue Date: 2020
Publisher: Springer
Citation: Plieva, A.T., Chalikidi, P.N., Gutnov, A.V., Turiev, A.M., Demidov, O.P., Aksenov, N.A., Magkoev, T.T., Abaev, V.T. Novel synthetic approach to pyrrolo[1,2-b]cinnolines // Chemistry of Heterocyclic Compounds. - 2020. - Volume 56. - Issue 8. - Pages 1030-1041
Series/Report no.: Chemistry of Heterocyclic Compounds
Abstract: Straightforward method for the synthesis of pyrrolo[1,2-b]cinnolines starting from 2-nitrobenzaldehydes and 2-methylfurans has been elaborated. The key steps of the process are oxidative furan ring opening with diazonium cation and intramolecular alkylation of azo group of the resulted cinnoline with secondary allyl alcohol
URI: http://hdl.handle.net/20.500.12258/14300
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:
File Description SizeFormat 
scopusresults 1407 .pdf
  Restricted Access
1.44 MBAdobe PDFView/Open
WoS 916 .pdf
  Restricted Access
77.25 kBAdobe PDFView/Open


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.