废止
对映体药物
对映选择合成
化学
卡宾
催化作用
组合化学
有机化学
立体化学
作者
Jiahan Li,Xiaoyong Duan,Xiaojie Ren,Yanting Li,Jing Qi
标识
DOI:10.1021/acs.joc.3c00793
摘要
An enantioselective construction of pyrazolo[3,4-b]pyridones was achieved via N-heterocyclic carbene-catalyzed [3 + 3] annulation of enals with 5-aminopyrazoles. This protocol not only offers a highly efficient synthetic approach for the preparation of various substituted pyrazolo[3,4-b]pyridones but also provides an effective method for the rapid synthesis of enantiopure spirooxindone derivatives.
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