Pothikumar Rajagopal, Sivaraj Chandrasekaran, Giridharan Kayambu, Ravva Mahesh Kumar, Namitharan Kayambu
Organic Synthesis and Catalysis Laboratory, Department of Chemistry, SRM Research Institute, SRM Institute of Science and Technology, Chennai 603 203, India.
Department of Chemistry, SRM University-AP, Amaravati, Andhra Pradesh 522502, India.
Org Lett. 2022 Jun 24;24(24):4310-4315. doi: 10.1021/acs.orglett.2c01180. Epub 2022 Jun 13.
Herein, we report a copper/amine catalyzed stereoselective addition of alkynes to ketenimine intermediates generated in situ from the sulfonyl azide-alkyne cycloaddition cascade for the stereoselective synthesis of ()-1,3-enynes. Significantly, for the first-time, enamine intermediates generated in the copper-catalyzed sulfonyl azide-alkyne cycloaddition reactions have been successfully trapped and isolated as the products. Density functional theory computations have also been performed and found to be consistent with the observed experimental stereoselectivity.
在此,我们报道了一种铜/胺催化的炔烃与由磺酰叠氮-炔烃环加成串联反应原位生成的烯酮亚胺中间体的立体选择性加成反应,用于立体选择性合成()-1,3-烯炔。值得注意的是,首次成功捕获并分离了铜催化的磺酰叠氮-炔烃环加成反应中生成的烯胺中间体作为产物。还进行了密度泛函理论计算,结果与观察到的实验立体选择性一致。