对映选择合成
化学
铱
芳基
叶立德
烷基化
级联反应
亚硝基
甲亚胺叶立德
组合化学
串联
立体化学
有机化学
环丙烷化
烯胺
酒
手性(物理)
药物化学
路易斯酸
有机合成
催化作用
手性助剂
奥西多尔
阿托品
作者
Yazhou Lin,Shanshan Yuan,Yu Xu,Hai Hu,Xiaoming Zhao,Y.-M. Liang,Sheng‐Cai Zheng
标识
DOI:10.1002/anie.202519102
摘要
The asymmetric functionalization of indoles at the C2 position to afford chiral tertiary alcohols poses a formidable challenge in organic synthesis, primarily due to the inherent preference for C3 reactivity. Herein, we report the asymmetric generation and transformation of carbonyl ylides from oxindoles using a β-aryl axially chiral iridium porphyrin complex. This system enables a highly site-selective and enantioselective reaction between oxindoles and aryl diazoesters, involving enantioselective carbonyl ylide formation, tandem epoxidation, and rearrangement. The process efficiently provides a series of chiral tertiary 2-indolyl alcohols that are difficult to access via direct Friedel-Crafts alkylation of indoles.
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