Affiliation:
1. College of Chemistry and Chemical Engineering Qingdao University Ningxia Road 308# Qingdao 266071 China
2. School of Chemistry and Chemical Engineering Shandong University Jinan 250100 China
Abstract
AbstractNickel‐catalyzed transannulation reactions triggered by the extrusion of small gaseous molecules have emerged as a powerful strategy for the efficient construction of heterocyclic compounds. However, their use in asymmetric synthesis remains challenging because of the difficulty in controlling stereo‐ and regioselectivity. Herein, we report the first nickel‐catalyzed asymmetric synthesis of N−N atropisomers by the denitrogenative transannulation of benzotriazones with alkynes. A broad range of N−N atropisomers was obtained with excellent regio‐ and enantioselectivity under mild conditions. Moreover, density functional theory (DFT) calculations provided insights into the nickel‐catalyzed reaction mechanism and enantioselectivity control.
Funder
National Natural Science Foundation of China
Taishan Scholar Foundation of Shandong Province
Natural Science Foundation of Shandong Province
Science and Technology Support Plan for Youth Innovation of Colleges and Universities of Shandong Province of China
Cited by
2 articles.
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