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Highly efficient and stereoselective cycloaddition of nitrones to indolyl- and pyrrolylacrylates
Authors:Viktor A Dmitriev  Mariia M Efremova  Alexander S Novikov  Vladimir V Zarubaev  Alexander V Slita  Anastasia V Galochkina  Galina L Starova  Andrey V Ivanov  Alexander P Molchanov
Institution:1. Saint Petersburg State University, Universitetskaya nab. 7/9, St. Petersburg 199034, Russian Federation;2. Pasteur Institute of Epidemiology and Microbiology, 14 Mira Str., 197101 St. Petersburg, Russian Federation;3. A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Sciences, 1 Favorsky Str., Irkutsk 664033, Russian Federation
Abstract:The reactions of various nitrones with indolyl- and pyrrolylacrylates proceeds regioselectively with high diastereoselectivity in the case of aldonitrones, and represents an effective method for obtaining new indolyl- and pyrrolyl-substituted isoxazolidine carboxylates stabilized by weak (C/>H?O) and moderate (N<img style=
Keywords:XYLXZWGMPCFNNK-NCPLZGKYSA-N  FGYPTCUVKNZGLP-HUYTWLNPSA-N  KXTPJVBHRNRVNY-PWHSHALESA-N  SQOUCQYYQYHGOQ-CMDGGOBGSA-N  UYUNGRNZQQYXRA-PKNBQFBNSA-N  VJJVQHRZOUYRNC-RMTZWNOUSA-N  JXRLXVDXJMURBS-CMTIAEDTSA-N  IYMDGZMPSGMTKI-FULLSBAXSA-N  DPOGIPKDAYEYER-QSJYAPKHSA-N  VSJPSUROITXSFJ-CMTIAEDTSA-N  MGEFQWWXYIOVHT-FULLSBAXSA-N  HMENNZUAPIELMS-FULLSBAXSA-N  HJBIRYYHCWTNLW-IUAQSZDVSA-N  XYLXZWGMPCFNNK-UBFVSLLYSA-N  YHNUCZBTRIFIHD-UBFVSLLYSA-N  AOGJCKTZQHAJKT-TWJOJJKGSA-N  MIZJAJSRTQRGJO-WOJBJXKFSA-N  OSJCBCPUPDRLAE-WOJBJXKFSA-N  ZYZLMDNUHBMZRL-NHCUHLMSSA-N  ZEXUEJYFCYWMAP-SDVJBAMBSA-N  KXTPJVBHRNRVNY-DNVFCKCGSA-N  Indoles  Cycloaddition  Nitrones  Isoxazolidines
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