Shen Yao-Bin, Qian Hui-Ling, Yang Lei, Zhou Shun, Rao Han-Wen, Wang Zhen-Hua, You Yong, Zhang Yan-Ping, Yin Jun-Qing, Zhao Jian-Qiang, Zhang Wenjing, Yuan Wei-Cheng
Innovation Research Center of Chiral Drugs, Institute for Advanced Study, Chengdu University, Chengdu 610106, China.
College of Chemistry, Chemical Engineering and Materials Science, Zaozhuang University, Zaozhuang 277160, China.
Org Lett. 2024 Mar 1;26(8):1699-1704. doi: 10.1021/acs.orglett.4c00227. Epub 2024 Feb 22.
The first direct catalytic asymmetric Mannich reaction of 2-alkylazaarenes and ketimines was realized with a chiral Cu-bis(oxazoline) complex as the catalyst. The asymmetric addition of 2-alkylpyridines to isatin-derived ketimines proceeded smoothly to afford α,β-functionalized 2-substituted pyridines bearing 3-amino-3,3-disubstituted oxindole motifs with excellent results (≤99% yield, 99:1 dr, and 98% ee). The catalytic system was also extended to 2-alkylbenzothiazoles as nucleophiles for the asymmetric Mannich reaction of ketimines.
首次以手性铜双恶唑啉配合物为催化剂实现了2-烷基氮杂芳烃与酮亚胺的直接催化不对称曼尼希反应。2-烷基吡啶与异吲哚酮衍生的酮亚胺的不对称加成反应顺利进行,得到了带有3-氨基-3,3-二取代氧化吲哚基序的α,β-官能化2-取代吡啶,结果优异(产率≤99%,非对映体比例为99:1,对映体过量值为98%)。该催化体系还扩展至以2-烷基苯并噻唑作为亲核试剂用于酮亚胺的不对称曼尼希反应。