Fig. 1: Transition-metal-catalyzed difunctionalization of olefin and arene. | Nature Communications

Fig. 1: Transition-metal-catalyzed difunctionalization of olefin and arene.

From: Dearomative 1,4-difunctionalization of naphthalenes via palladium-catalyzed tandem Heck/Suzuki coupling reaction

Fig. 1: Transition-metal-catalyzed difunctionalization of olefin and arene.The alternative text for this image may have been generated using AI.

a TM-catalyzed difunctionalization of alkene (well-developed)2,9,10,11,12,13,14,15,16. b Dearomative difunctionalization of naphthalene or benzene (unknown). c Dearomative 1,4-diarylation/vinylarylation of naphthalenes via Heck/Suzuki coupling (This work). [M] metal catalyst, Nu nucleophile, L ligand, L′ linker, Ar arene.

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