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
AUTHORS (7)
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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