Total synthesis of buergerinin F via effective construction of the asymmetric quaternary carbons using an enantioselective aldol reaction.
نویسندگان
چکیده
An efficient method for the synthesis of (+)-buergerinin F is established via the enantioselective aldol reaction of a tetra-substituted ketene silyl acetal with crotonaldehyde, followed by intramolecular Wacker-type ketalization.
منابع مشابه
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ورودعنوان ژورنال:
- Chemical communications
دوره 32 شماره
صفحات -
تاریخ انتشار 2005