化学
炔烃
催化作用
恶嗪类
区域选择性
立体选择性
组合化学
芳基
碘
喹唑啉
有机化学
烷基
作者
Wen‐Chun Lee,Ho‐Chuan Shen,Wenli Hu,Wei‐Sheng Lo,Chebrolu Murali,Jaya Kishore Vandavasi,Jeh‐Jeng Wang
标识
DOI:10.1002/adsc.201200018
摘要
Abstract 4‐Benzylidene‐2‐aryl‐4 H ‐benzo[ d ][1,3] oxazines have been synthesized with high stereoselectivity and regioselectivities from 2‐alkynylbenzamides in the presence of a catalytic amount of I 2 . In the reaction mechanism, iodine plays a key role in two different aspects as a catalyst, such as to activate the alkyne with the iodinium donor which triggers the cascade, and then as a proper acid source to facilitate catalyst recovery. The benzoxazines have been exploited as potential substrates for the synthesis of quinazoline 3‐oxide derivatives directly in one step.
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