Iridium-Catalyzed Regio- and Enantioselective N-Allylation of Pyrazoles with Dienyl/Monoallylic Alcohols

被引:3
|
作者
Zhang, Peng [1 ]
Zhang, Yulu [1 ]
Shao, Ying [1 ]
Sun, Jiangtao [1 ]
Tang, Shengbiao [1 ]
机构
[1] Changzhou Univ, Sch Petrochem Engn, Jiangsu Key Lab Adv Catalyt Mat & Technol, Changzhou 213164, Peoples R China
基金
中国国家自然科学基金;
关键词
PRIMARY ALLYLIC AMINES; AMINATION; SUBSTITUTION; ALKYLATION; ACCESS;
D O I
10.1021/acs.orglett.4c01201
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Here we report the first example of iridium-catalyzed asymmetric N-allylation of pyrazoles with dienyl allylic alcohols under mild conditions with broad functional group tolerance, exhibiting excellent N-1/C3-site selectivities and enantioselectivities (up to >99% ee). In addition to pyrazoles, other nucleophiles including benzotriazole, triazole, and pyrazole precursors (aryl vinyldiazos) are also suitable in this method. Notably, with the use of Sc(OTf)(3) as additive and reactions performed at 30 degree celsius for 24 h, the N-1-C5 or N-1-C1 selective alkylated pyrazoles are also obtained.
引用
收藏
页码:3966 / 3971
页数:6
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