Citation: Zhang Gaopeng, Jiang Yangjie, Ding Changhua, Hou Xuelong. Palladium-Catalyzed Allylic Alkylation Reaction of α-Substituted Benzyl Nitriles with Branched Allyl Carbonates[J]. Chinese Journal of Organic Chemistry, ;2020, 40(10): 3399-3409. doi: 10.6023/cjoc202006007 shu

Palladium-Catalyzed Allylic Alkylation Reaction of α-Substituted Benzyl Nitriles with Branched Allyl Carbonates

Zhang Gaopeng ^a,d ,
Jiang Yangjie ^a,d ,
Ding Changhua ^b,, ,
Hou Xuelong ^a,c,,

a.
State Key Laboratory of Organometallic Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032
b.
Department of Chemistry, Shanghai University, Shanghai 200032
c.
Shanghai-Hong Kong Joint Laboratory in Chemical Synthesis, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, Shanghai 200032
d.
University of Chinese Academy of Sciences, Beijing 100049

Corresponding author: Ding Changhua, dingchanghua@shu.edu.cn Hou Xuelong, xlhou@sioc.ac.cn
Received Date: 5 June 2020
Revised Date: 23 June 2020
Available Online: 30 June 2020
Fund Project: the National Natural Science Foundation of China 21532010the Strategic Priority Research Program of the Chinese Academy of Sciences XDB20030100the National Natural Science Foundation of China 21772215Project supported by the National Natural Science Foundation of China (Nos. 21532010, 21772215), the Strategic Priority Research Program of the Chinese Academy of Sciences (No. XDB20030100), the Chinese Academy of Sciences, the Technology Commission of Shanghai Municipality, and the Croucher Foundation of Hong Kong

Figures(4)

Pd-catalyzed allylic alkylation reaction of α-substituted benzyl nitriles with branched allyl carbonates in the presence of bulkier N-heterocyclic carbene ligand was reported, which provided the corresponding allylated products in good yield with high regio- and diastereo-selectivity.
- palladium,
- benzyl nitriles,
- branched allyl carbonates,
- allylic alkylation reaction
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