化学
脱质子化
烯丙基重排
筑地反应
催化作用
烷基化
取代基
对映选择合成
组合化学
基质(水族馆)
三乙胺
烷基
共轭体系
药物化学
有机化学
反应条件
作者
Qi-Fei Liu,Qianqian Peng,Shifeng Hao,Lu Liu,Fu-Hao Zhang,Zhu-Jun Shi,Jian‐Hua Xie,Chongren Ai,Xiaochen Wang
摘要
Asymmetric functionalization of unactivated alkyl-substituted azaarenes at the α-position of the alkyl substituent is challenging because deprotonation of the weakly acidic α-C-H bonds requires a strong base. This requirement often impedes effective enantiocontrol by chiral catalysts. As a result, the few reactions that have been reported have narrow substrate scopes. Herein, we report a method for highly diastereo- and enantioselective allenylic alkylation reactions of unactivated 2-alkylbenzoxazoles with conjugated enynes, enabled by synergistic borane/nickel catalysis. The success of this method hinges on catalytic activation of the 2-alkylbenzoxazoles by a triarylborane, which permits deprotonation by triethylamine and thus is crucial for achieving both high yields and diastereo- and enantioselectivities. Extending the utility of synergistic borane/transition metal catalysis, we also demonstrate that a borane/palladium system effectively overcomes the limitations of palladium-catalyzed allylic alkylation reactions of unactivated azaarenes. In particular, previously unreactive acyclic 1,3-disubstituted allylic esters are rendered viable electrophiles, enabling the construction of products bearing two adjacent stereocenters.
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