Pd-Catalyzed Asymmetric [3+4] Cycloaddition of Trimethylene-methane: Highly Regio-, Diastereo-, and Enantio-selective Construction of Benzofuro[3,2-b]azepines

doi:10.6023/cjoc202000014

Chinese Journal of Organic Chemistry ›› 2020, Vol. 40 ›› Issue (3): 812-813.DOI: 10.6023/cjoc202000014 Previous Articles Next Articles

钯催化三亚甲基甲烷的不对称[3＋4]环加成反应:高区域选择性、高非对映选择性和高对映选择性构筑苯并呋喃[3,2-b]吖庚因

王美馨, 邓玉华, 邵志会

云南大学化学科学与工程学院教育部自然资源药物化学重点实验室昆明 650091

发布日期:2020-04-02
通讯作者: 邓玉华, 邵志会 E-mail:dengyuhua@ynu.edu.cn;zhihui_shao@hotmail.com

Pd-Catalyzed Asymmetric [3+4] Cycloaddition of Trimethylene-methane: Highly Regio-, Diastereo-, and Enantio-selective Construction of Benzofuro[3,2-b]azepines

Wang Meixin, Deng Yuhua, Shao Zhihui

Key Laboratory of Medicinal Chemistry for Natural Resource, Ministry of Education, School of Chemical Science and Technology, Yunnan University, Kunming 650091

Published:2020-04-02

Cite this article

Wang Meixin, Deng Yuhua, Shao Zhihui. Pd-Catalyzed Asymmetric [3+4] Cycloaddition of Trimethylene-methane: Highly Regio-, Diastereo-, and Enantio-selective Construction of Benzofuro[3,2-b]azepines[J]. Chinese Journal of Organic Chemistry, 2020, 40(3): 812-813.

钯催化三亚甲基甲烷的不对称[3＋4]环加成反应:高区域选择性、高非对映选择性和高对映选择性构筑苯并呋喃[3,2-b]吖庚因

Pd-Catalyzed Asymmetric [3+4] Cycloaddition of Trimethylene-methane: Highly Regio-, Diastereo-, and Enantio-selective Construction of Benzofuro[3,2-b]azepines

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