We developed a photocatalytic copper-catalyzed stereodivergent 3,4-hydroalkoxylation of 1,3-dienes. By simply controlling reaction time, this protocol selectively affords either E- or Z-allylic ethers in moderate to excellent yields with high stereoselectivity (up to >20/1). The transformation demonstrates remarkable scalability, maintaining excellent stereocontrol even at gram-scale operations. Preliminary mechanistic studies reveal: (1) initial SET reduction generates key diene radical anion intermediates, (2) a synergistic photoredox/copper catalytic manifold directs E-selectivity, and (3) prolonged irradiation induces EnT-mediated photoisomerization to the Z-products.
Yuan et al. (Mon,) studied this question.