Ruthenium Catalyzed C–H Selenylations of Aryl Acetic Amides and Esters via Weak Coordination

Functional group Coordination complex
DOI: 10.1021/acs.orglett.9b02196 Publication Date: 2019-08-05T13:05:06Z
ABSTRACT
An efficient ruthenium-catalyzed direct C-H selenylation of aryl acetic amides and esters has been achieved via distal weakly coordination. Notable features this protocol including broad substrate scope, wide functional group tolerance, good regioselectivity. In addition, diaryl disulfides were also successfully applied to reaction under slightly modified conditions.
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