Please use this identifier to cite or link to this item: https://dspace.ncfu.ru/handle/20.500.12258/12118
Title: Dipyrazolodioxadiazocines as shelf-stable "ready-to-use" precursors for an in situ generation of enolate-iminium 1,4-dipoles: a straightforward atom-economical approach to pyrazolo[5,1-d][1,3,5]dioxazines
Authors: Rubin, M. A.
Рубин, М. А.
Keywords: Dipyrazolodioxadiazocines;Atom economical;Atom-economical approach;Isoxazole derivative
Issue Date: 2020
Publisher: NLM (Medline)
Citation: Zhulanov, V.E., Vigovskaya, V.A., Dmitriev, M.V., Silaichev, P.S., Maslivets, A.N., Rubin, M. Dipyrazolodioxadiazocines as shelf-stable "ready-to-use" precursors for an in situ generation of enolate-iminium 1,4-dipoles: a straightforward atom-economical approach to pyrazolo[5,1-d][1,3,5]dioxazines // Organic & biomolecular chemistry. - 2020. - Volume 18. - Issue 17. - Pages 3382-3391
Series/Report no.: Organic and Biomolecular Chemistry
Abstract: An original, facile and highly efficient method for the in situ generation of cyclic enolate-iminium 1,4-dipoles via unique thermal decomposition of easily available dipyrazolodioxadiazocines has been developed. Various substituted pyrazolo[5,1-d][1,3,5]dioxazines have been prepared in high yields via unusual cycloconversion of dipyrazolodioxadiazocines in the presence of ketones. Furthermore, the developed method is 100% atom economical and proceeds under metal-, catalyst- and solvent-free conditions
URI: http://hdl.handle.net/20.500.12258/12118
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:
File Description SizeFormat 
scopusresults 1284 .pdf
  Restricted Access
2.03 MBAdobe PDFView/Open
WoS 824 .pdf
  Restricted Access
194.04 kBAdobe PDFView/Open


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