Preparation of enantiopure sultams by intramolecular Diels-Alder reaction of 1,3-cyclohexadiene-containing vinylsulfonamides

Victor O. Rogachev, Peter Metz

    Результат исследований: Материалы для книги/типы отчетовМатериалы для конференции

    Выдержка

    Enantiomerically pure δ-sultams have been prepared by intramolecular [4+2] cycloaddition of N-1-phenylethyl substituted vinylsulfonamides with purely thermal activation and under high pressure. An optimized procedure for reductive debenzylation of the resultant δ-sultams is also reported.

    Язык оригиналаАнглийский
    Название основной публикации8th Korea-Russia International Symposium on Science and Technology - Proceedings: KORUS 2004
    Страницы76-79
    Число страниц4
    Том2
    СостояниеОпубликовано - 2004
    Событие8th Korea-Russia International Symposium on Science and Technology, KORUS 2004 - Tomsk, Российская Федерация
    Продолжительность: 26 июн 20043 июл 2004

    Другое

    Другое8th Korea-Russia International Symposium on Science and Technology, KORUS 2004
    СтранаРоссийская Федерация
    ГородTomsk
    Период26.6.043.7.04

    Отпечаток

    Cycloaddition
    Chemical activation
    Hot Temperature

    ASJC Scopus subject areas

    • Engineering(all)

    Цитировать

    Rogachev, V. O., & Metz, P. (2004). Preparation of enantiopure sultams by intramolecular Diels-Alder reaction of 1,3-cyclohexadiene-containing vinylsulfonamides. В 8th Korea-Russia International Symposium on Science and Technology - Proceedings: KORUS 2004 (Том 2, стр. 76-79)

    Preparation of enantiopure sultams by intramolecular Diels-Alder reaction of 1,3-cyclohexadiene-containing vinylsulfonamides. / Rogachev, Victor O.; Metz, Peter.

    8th Korea-Russia International Symposium on Science and Technology - Proceedings: KORUS 2004. Том 2 2004. стр. 76-79.

    Результат исследований: Материалы для книги/типы отчетовМатериалы для конференции

    Rogachev, VO & Metz, P 2004, Preparation of enantiopure sultams by intramolecular Diels-Alder reaction of 1,3-cyclohexadiene-containing vinylsulfonamides. в 8th Korea-Russia International Symposium on Science and Technology - Proceedings: KORUS 2004. том. 2, стр. 76-79, Tomsk, Российская Федерация, 26.6.04.
    Rogachev VO, Metz P. Preparation of enantiopure sultams by intramolecular Diels-Alder reaction of 1,3-cyclohexadiene-containing vinylsulfonamides. В 8th Korea-Russia International Symposium on Science and Technology - Proceedings: KORUS 2004. Том 2. 2004. стр. 76-79
    Rogachev, Victor O. ; Metz, Peter. / Preparation of enantiopure sultams by intramolecular Diels-Alder reaction of 1,3-cyclohexadiene-containing vinylsulfonamides. 8th Korea-Russia International Symposium on Science and Technology - Proceedings: KORUS 2004. Том 2 2004. стр. 76-79
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    abstract = "Enantiomerically pure δ-sultams have been prepared by intramolecular [4+2] cycloaddition of N-1-phenylethyl substituted vinylsulfonamides with purely thermal activation and under high pressure. An optimized procedure for reductive debenzylation of the resultant δ-sultams is also reported.",
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