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Pd(II)-Catalyzed Carbonyl-Directing Activation of Alkenes: Selective Fluorosulfonylation and Aminosulfonylation of 1,7-Enynes

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NIAID Data Ecosystem2026-03-10 收录
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https://figshare.com/articles/dataset/Pd_II_-Catalyzed_Carbonyl-Directing_Activation_of_Alkenes_Selective_Fluorosulfonylation_and_Aminosulfonylation_of_1_7-Enynes/6962474
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A new Pd­(II)-catalyzed carbonyl-directing activation of alkenes has been established, enabling radical-induced selective fluorosulfonylation and aminosulfonylation of carbonyl-tethered 1,7-enynes with sulfinic acids and N-fluorobenzenesulfonimide (NFSI) under mild and redox neutral conditions to access densely functionalized (E)-3,4-dihydronaphthalen-1­(2H)-ones with generally good yields and high stereoselectivity. The selectivity of these bifunctionalizations relies on the electronic nature of substituents on both aryl rings of 1,7-enynes.
创建时间:
2018-08-13
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