Copper-Catalyzed Dynamic Kinetic Asymmetric Arylation of Secondary Phosphine-Boranes for the Synthesis of P(III)-Stereogenic Centers

被引:0
|
作者
Wang, Xue [1 ,2 ]
Jin, Xiao [1 ,2 ,3 ]
Ge, Lei [1 ,2 ]
Wang, Deyin [1 ,2 ]
Zhang, Chun [1 ,2 ,3 ]
Wang, Zhen [1 ,2 ,3 ]
Shi, Xiaowei [1 ,2 ,3 ]
Yang, Wenqiang [1 ,2 ,3 ]
机构
[1] Linyi Univ, Coll Med, Linyi 276000, Shandong, Peoples R China
[2] Linyi Univ, Coll Chem & Chem Engn, Linyi 276000, Shandong, Peoples R China
[3] Shandong Prov Key Lab Biol Preparat & Applicat Tec, Linyi 276000, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
P-STEREOGENIC PHOSPHINES; ENANTIOSELECTIVE SYNTHESIS; OXIDES; LIGANDS; ALKYLATION; HYDROPHOSPHINATION; STEREOCHEMISTRY; HETEROCYCLES; RESOLUTION; MECHANISM;
D O I
10.1021/acs.orglett.5c00682
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Transition-metal-catalyzed asymmetric C-P(III) bond formation is a direct method for the construction of P(III)-stereogenic centers; however, achieving high enantioselectivity remains a challenge. Herein, an unprecedented Cu-catalyzed dynamic kinetic resolution of secondary phosphine-boranes was successfully developed. This asymmetric C-P(BH3) coupling reaction provided the direct and highly enantioselective synthesis of P(III)-stereogenic centers, enabling the formation of chiral medium-sized benzophosphine-boranes (7-10-membered cycles). A mechanism of dynamic kinetic resolution involving the unusual rapid racemization of secondary phosphine-boranes has been proposed.
引用
收藏
页码:3024 / 3030
页数:7
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