Please use this identifier to cite or link to this item: http://hdl.handle.net/20.500.12258/3532
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 (Cambridge, England)
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
URI: https://www.scopus.com/record/display.uri?eid=2-s2.0-85056941680&origin=resultslist&sort=plf-f&src=s&nlo=1&nlr=20&nls=afprfnm-t&affilName=north+caucasus+federal+university&sid=daa86f0573a9fe8189fcdb08cc741e58&sot=afnl&sdt=sisr&sl=53&s=%28AF-ID%28%22North+Caucasus+Federal+University%22+60070541%29%29&ref=%28Nitrostyrenes+as+1%2c4-CCNO-dipoles%3a+diastereoselective+formal+%5b4%2b1%5d+cycloaddition+of+indoles%29&relpos=0&citeCnt=0&searchTerm=
http://hdl.handle.net/20.500.12258/3532
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