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
冶金
材料科学
作者
Wei Huang,Jiahui Bai,Yinlong Guo,Qinglei Chong,Fanke Meng
出处
期刊:Angewandte Chemie
[Wiley]
日期:2023-03-03
卷期号:62 (19): e202219257-e202219257
被引量:33
标识
DOI:10.1002/anie.202219257
摘要
Abstract 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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