Please use this identifier to cite or link to this item:
Title: Nitrostyrenes as 1,4-CCNO-dipoles: diastereoselective formal [4+1] cycloaddition of indoles
Authors: Aksenov, A. V.
Аксенов, А. В.
Aksenov, N. A.
Аксенов, Н. А.
Aksenov, D. A.
Аксенов, Д. А.
Khamraev, V. F.
Хамраев, В. Ф.
Rubin, M. A.
Рубин, М. А.
Keywords: Indole;Cycloaddition of indoles
Issue Date: 2018
Publisher: NLM (Medline)
Citation: Aksenov, A.V., Aksenov, N.A., Aksenov, D.A., Khamraev, V.F., Rubin, M. Nitrostyrenes as 1,4-CCNO-dipoles: diastereoselective formal [4+1] cycloaddition of indoles // Chemical communications (Cambridge, England). - 2018. - Volume 54. - Issue 94. - Pages 13260-13263
Series/Report no.: Chemical communications
Abstract: An unusual reactivity of nitrostyrenes in phosphorous acid was discovered, which permits the employment of these readily available synthons as 1,4-CCNO-dipole surrogates in a highly diastereoselective (4+1)-cycloaddition of indoles to afford 4'H-spiro[indole-3,5'-isoxazoles] in a diastereomerically pure form
Appears in Collections:Статьи, проиндексированные в SCOPUS, WOS

Files in This Item:
File Description SizeFormat 
scopusresults 631 .pdf2.3 MBAdobe PDFThumbnail
WoS 416 .pdf106.75 kBAdobe PDFThumbnail

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