Sulfoximine-Directed Ruthenium-Catalyzed ortho-C鈥揌 Alkenylation of (Hetero)Arenes: Synthesis of EP3 Receptor Antagonist Analogue
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文摘
The reusable sulfoximine directing-group-assisted Ru(II)-catalyzed chemo- and regioselective ortho-C鈥揌 alkenylation of arenes and heteroarenes with acrylates and 伪,尾-unsaturated ketones/vinyl sulfone is shown. The N-aroyl sulfoximine undergoes annulation with diphenylacetylene, delivering isoquinolinones and methyl phenyl sulfoxide. The present protocol is successfully employed for the synthesis of the EP3 receptor antagonist analogue.

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