Decarboxylative allylations of ester enolate equivalents.
نویسندگان
چکیده
A variety of ester enolate equivalents are generated in situ and undergo α-allylation in high yields via palladium-catalyzed decarboxylative allylation. The transformations are complete within very short reaction times under ambient conditions. Synthesis of α-allylated acyl derivatives provides access to other carboxylic acid and alcohol derivatives via acyl group substitution or reduction.
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ورودعنوان ژورنال:
- Organic & biomolecular chemistry
دوره 12 42 شماره
صفحات -
تاریخ انتشار 2014