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◆ The Journal of organic chemistry2026-09-04

Photocatalytic Fluorosulfonylmethylation/Fluorosulfonylation of 2-Amino Aryl Ethynes to Access Dibenzazepine-/Dioxodibenzothiazepine-Functionalized Allyl/Vinyl Sulfonyl Fluorides.

Jian-Hong Zhang, Yun-Qi Lin, Ye-Pu Fu, Yan-Hui Li, Jun-Zhao Ma, Lele Zhang, Wei Li, Li-Jing Wang

原始摘要(英文原文)· Original abstract
This study reports a simple and efficient photocatalytic radical cascade cyclization strategy for the one-step synthesis of allyl- and vinyl-sulfonyl fluorides bearing dibenzazepine or dioxodibenzothiazepine scaffolds. In contrast to the existing synthesis methods of allyl sulfonyl fluoride, this approach employs aryl-terminal alkynes as starting materials, thereby avoiding the reliance on preformed allylic frameworks. The reaction utilizes inexpensive and readily accessible -CH2SO2F and -SO2F precursors, exhibits a broad substrate scope, proceeds under mild conditions, and delivers high stereoselectivity. The synthetic utility of this methodology was further demonstrated through SuFEx-based ligation with other molecules.
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Photocatalytic Fluorosulfonylmethylation/Fluorosulfonylation of 2-Amino Aryl Ethynes to Access Dibenzazepine-/Dioxodibenzothiazepine-Functionalized Allyl/Vinyl Sulfonyl Fluorides. — 科研速览 Science Skim