对映选择合成
区域选择性
烯丙基重排
催化作用
化学
磷化氢
质子化
立体选择性
组合化学
产量(工程)
试剂
有机化学
药物化学
离子
材料科学
冶金
作者
Wei Huang,Jiahui Bai,Yinlong Guo,Qinglei Chong,Fanke Meng
标识
DOI:10.1002/anie.202219257
摘要
Catalytic enantioselective coupling of 1,1-disubstituted allenes and aldehydes through regiodivergent oxidative cyclization followed by stereoselective protonation or reductive elimination promoted by chiral phosphine-Co complexes is presented. Such processes represent unprecedented and unique reaction pathways for Co catalysis that enable catalytic enantioselective generation of metallacycles with divergent regioselectivity accurately controlled by chiral ligands, affording a wide range of allylic alcohols and homoallylic alcohols that are otherwise difficult to access without the need of pre-formation of stoichiometric amounts of alkenyl- and allyl-metal reagents in up to 92 % yield, >98 : 2 regioselectivity, >98 : 2 dr and >99.5 : 0.5 er.
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