Abstract:An efficient and straightforward protocol for the regioselective acyloxylation of N-arylarbamates via Pd-catalyzed CÀ H bond functionalization has been demonstrated. The aliphatic and benzoic acid derivatives were used as the acyloxyl source to convert aromatic sp 2 CÀ H bonds into CÀ O bonds. Additionally, the oxidative homocoupling of N-arylarbamates were evaluated and gave the corresponding homocoupled products in good yields.
“…To continue our research interest aiming at N ‐heterocycle directed C–H bond functionalization of arenes, herein, we report the first Pd‐catalyzed C–H activation/sulfonylation and halogenation reactions of phthalazindiones. These approaches afford predominantly mono ‐functionalized products under mild and oxidant‐free reaction conditions using a palladium catalytic system and readily accessible and inexpensive reagents as functional group sources (Scheme h).…”
The regio-and chemo-selective Pd-catalyzed C-H activation methods have been successfully reported for directed C-H sulfonation and halogenation of pyridazinedione with arylsulfonyl chlorides and N-halosuccinimide, respectively. These [a]
“…To continue our research interest aiming at N ‐heterocycle directed C–H bond functionalization of arenes, herein, we report the first Pd‐catalyzed C–H activation/sulfonylation and halogenation reactions of phthalazindiones. These approaches afford predominantly mono ‐functionalized products under mild and oxidant‐free reaction conditions using a palladium catalytic system and readily accessible and inexpensive reagents as functional group sources (Scheme h).…”
The regio-and chemo-selective Pd-catalyzed C-H activation methods have been successfully reported for directed C-H sulfonation and halogenation of pyridazinedione with arylsulfonyl chlorides and N-halosuccinimide, respectively. These [a]
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