DOI: 10.1021/acsappcat.6c00118 ISSN: 3071-4559

Simultaneous Two-Directional Catalytic Radical Cross-Coupling

Joshua O. Imasuen, Baiyang Jiang, Manolis Sofiadis, Kaid C. Harper, Daiki Yamamoto, Tomoya Imai, Alexandros S. Pollatos, Philipp Neigenfind, Yu Kawamata, Phil S. Baran

Abstract

Two-directional synthesis is a powerful strategy for rapidly increasing molecular complexity, yet its tactical implementation with radical cross-coupling remains underdeveloped. Here, we report simultaneous two-directional radical cross-coupling of bifunctional radical precursors. Diacid-derived bis-redox-active esters undergo Ag–Ni electrocatalytic decarboxylative arylation to access functionalized dibenzyl amines and related linkers, while diamine-derived bis-sulfonyl hydrazides participate in redox-neutral deaminative RCC. This strategy enables chemoselective, scalable access to valuable products from readily available starting materials.

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