Direct access to isoindolines through tandem Rh(III)-catalyzed alkenylation and cyclization of N-benzyltriflamides.
نویسندگان
چکیده
The rhodium-catalyzed oxidative alkenylation of N-benzyltriflamides with olefins followed by an intramolecular cyclization via C-H bond activation is described. This method results in the direct and efficient synthesis of highly substituted isoindoline frameworks.
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ورودعنوان ژورنال:
- Chemical communications
دوره 50 18 شماره
صفحات -
تاریخ انتشار 2014