化学
铱
对映选择合成
催化作用
有机化学
组合化学
药物化学
立体化学
作者
Peng Zhang,Yulu Zhang,Ying Shao,Jiangtao Sun,Shengbiao Tang
出处
期刊:Organic Letters
[American Chemical Society]
日期:2024-04-26
卷期号:26 (18): 3966-3971
被引量:12
标识
DOI:10.1021/acs.orglett.4c01201
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 N1/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 °C for 24 h, the N1-C5 or N1-C1 selective alkylated pyrazoles are also obtained.
科研通智能强力驱动
Strongly Powered by AbleSci AI