Highly chemoselective copper-catalyzed conjugate reduction of stereochemically labile alpha,beta-unsaturated amino ketones.
نویسندگان
چکیده
Highly chemoselective conjugate reduction of chiral alpha,beta-unsaturated amino ketones has been developed by using triisopropyl phosphite ligated copper hydride complex. The highlights of the method are wide substrate compatibility and exceptional chemoselectivity.
منابع مشابه
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ورودعنوان ژورنال:
- The Journal of organic chemistry
دوره 74 19 شماره
صفحات -
تاریخ انتشار 2009