This review describes the overview of mechanistic and kinetics insights for guiding the design of catalysts for selective hydrogenation of functionalized nitroarenes to produce anilines, and summarizes the strategies developed for controlling the...
Artikel
Palladium‐Catalyzed C−H Alkenylation of α‐Aryl Alkyl Nitriles
Von Wiley-VCH zur Verfügung gestellt
The direct α-alkenylation of nitrile was realized with palladium catalyst for the first time. Both cyano group and alkenyl group in the product can be functionalized, rendering this method a powerful protocol to synthesis a series of useful compounds.
Abstract
A direct α-alkenylation of nitrile compounds was realized with a palladium complex. This method exhibited excellent tolerance toward a variety of α-aryl alkyl nitriles and vinyl bromides, leading to the formation of a series of α-quaternary nitriles containing vinyl groups. Further manipulations of the obtained products were demonstrated, highlighting the potential synthetic utility of this method.
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