The Domino Chromone Annulation and a Transient Halogenation-Mediated C-H Alkenylation toward 3-Vinyl Chromones

被引:91
作者
Fu, Leiqing [1 ,2 ]
Xu, Zhongrong [1 ]
Wan, Jie-Ping [1 ]
Liu, Yunyun [1 ]
机构
[1] Jiangxi Normal Univ, Coll Chem & Chem Engn, Nanchang 330022, Jiangxi, Peoples R China
[2] Yichun Univ, Coll Chem & Bioengn, Yichun 336000, Jiangxi, Peoples R China
基金
中国国家自然科学基金;
关键词
CROSS-COUPLING REACTIONS; TETRASUBSTITUTED OLEFINS; EFFICIENT SYNTHESIS; GENERAL-APPROACH; BOND ACTIVATION; FUNCTIONALIZATION; ARYLATION; ALKENES; DERIVATIVES; ENAMINONES;
D O I
10.1021/acs.orglett.0c03548
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Reported in this paper is a step economical method toward the general synthesis of 3-vinyl chromones via the reactions between readily available o-hydroxyphenyl enaminones and various alkenes. The domino C-H alkenylation and chromone annulation of the enaminones are involved, which enables the synthesis of 3-vinyl chromone products using both terminal and internal alkenes via a key process of transient C-H halogenation.
引用
收藏
页码:9518 / 9523
页数:6
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