Reductive Alkylation of Alkenyl Acetates with Alkyl Bromides by Nickel Catalysis

被引:34
作者
He, Rong-De [1 ]
Bai, Yunfei [1 ]
Han, Guan-Yu [1 ]
Zhao, Zhen-Zhen [1 ]
Pang, Xiaobo [1 ]
Pan, Xiaobo [1 ]
Liu, Xue-Yuan [1 ]
Shu, Xing-Zhong [1 ]
机构
[1] Lanzhou Univ, Coll Chem & Chem Engn, State Key Lab Appl Organ Chem SKLAOC, 222 South Tianshui Rd, Lanzhou 730000, Peoples R China
基金
中国国家自然科学基金;
关键词
Alkenes; Alkenylation; Alkylation; Cross-coupling; Nickel; CROSS-COUPLING REACTIONS; ARYL HALIDES; C-O; ENANTIOSELECTIVE SYNTHESIS; VINYL; DERIVATIVES; ACTIVATION; REAGENTS; NI; ELECTROPHILES;
D O I
10.1002/anie.202114556
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Catalytic alkylation of stable alkenyl C-O electrophiles is synthetically appealing, but studies to date have typically focused on the reactions with alkyl Grignard reagents. We report herein a cross-electrophile reaction of alkenyl acetates with alkyl bromides. This work has enabled a new method for the synthesis of aliphatic alkenes from alkenyl acetates to be established that can be used to add more structural complexity and molecular diversity with enhanced functionality tolerance. The method allows for a gram-scale reaction and modification of biologically active molecules, and it affords access to useful building blocks. Preliminary mechanistic studies reveal that the Ni-I species plays an essential role for the success of the coupling of these two reactivity-mismatched electrophiles.
引用
收藏
页数:6
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