苯并噻二嗪
对映选择合成
化学
钴
催化作用
键裂
组合化学
羧酸
药物化学
有机化学
立体化学
作者
Yuuki Hirata,Daichi Sekine,Yoshimi Kato,Luqing Lin,M. Kojima,Tatsuhiko Yoshino,Shigeki Matsunaga
标识
DOI:10.1002/ange.202205341
摘要
Abstract Among sulfoximine derivatives containing a chiral sulfur center, benzothiadiazine‐1‐oxides are important for applications in medicinal chemistry. Here, we report that the combination of an achiral cobalt(III) catalyst and a pseudo‐ C 2 ‐symmetric H 8 ‐binaphthyl chiral carboxylic acid enables the asymmetric synthesis of benzothiadiazine‐1‐oxides from sulfoximines and dioxazolones via enantioselective C−H bond cleavage. With the optimized protocol, benzothiadiazine‐1‐oxides with several functional groups can be accessed with high enantioselectivity.
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