中国化学快报(英文版)2024,Vol.35Issue(8) :282-287.DOI:10.1016/j.cclet.2024.109518

One stone three birds:Ni-catalyzed asymmetric allenylic substitution of allenic ethers,hydroalkylation of 1,3-enynes and double alkylation of enynyl ethers

Zhirong Yang Shan Wang Ming Jiang Gengchen Li Long Li Fangzhi Peng Zhihui Shao
中国化学快报(英文版)2024,Vol.35Issue(8) :282-287.DOI:10.1016/j.cclet.2024.109518

One stone three birds:Ni-catalyzed asymmetric allenylic substitution of allenic ethers,hydroalkylation of 1,3-enynes and double alkylation of enynyl ethers

Zhirong Yang 1Shan Wang 1Ming Jiang 1Gengchen Li 1Long Li 1Fangzhi Peng 1Zhihui Shao1
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作者信息

  • 1. Key Laboratory of Medicinal Chemistry for Natural Resource,Ministry of Education,School of Chemical Science and Technology,Yunnan Provincial Center for Research & Development of Natural Products,and State Key Laboratory for Conservation and Utilization of Bio-Resources in Yunnan,Yunnan University,Kunming 650091,China
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Abstract

The development of low-cost,earth-abundant and environmentally benign transition metal catalysts,which can catalyze multiple different types of asymmetric reactions,is an important objective in mod-ern asymmetric catalysis.Herein we demonstrate that a chiral Ni/P-Phos catalyst achieves three types of asymmetric reactions:allenylic substitution of racemic allenic ethers,1,4-hydroalkylation of prochiral 1,3-enynes and double alkylation of newly designed enynyl ether reagents.Three methods complement each other and produce various axially chiral allene derivatives bearing a pyrazolidine-3,5-dione unit,which is widely present in drugs and biologically active molecules with versatile pharmacological activities.

Key words

Nickel Asymmetric catalysis/Allenylic substitution/Hydroalkylation/Double alkylation/Allene/1,3-Enyne/Pyrazolidine-3,5-dione

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出版年

2024
中国化学快报(英文版)
中国化学会

中国化学快报(英文版)

CSTPCD
影响因子:0.771
ISSN:1001-8417
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