化学
部分
炔烃
烯烃
催化作用
戒指(化学)
基质(水族馆)
组合化学
立体化学
功能群
药物化学
有机化学
海洋学
地质学
聚合物
作者
Ruiwen Jin,Jinjin Chen,Yiyong Chen,Wangsheng Liu,Dawen Xu,Yawei Li,Aishun Ding,Hao Chi Guo
标识
DOI:10.1021/acs.joc.6b02537
摘要
The first 6π-photocyclization of dienynes was developed, which provides a new and effective protocol for the synthesis of the phenyl ring in excellent yields with nice functional group tolerance. In this transformation, the Cu(OTf) 2 catalyst plays a key role in the conversion of alkyne moiety into an alkene-type moiety, which means that the dienyne reactant is converted into a triene-type substrate. Thus, this reaction proceeds via a Cu(II)-catalyzed 6π-photocyclization of triene-type derivatives.
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