化学
分子内力
异恶唑
催化作用
杂原子
戒指(化学)
组合化学
亲电芳香族取代
串联
阳离子聚合
区域选择性
接受者
电泳剂
药物化学
立体化学
有机化学
物理
复合材料
材料科学
凝聚态物理
作者
Taiki Morita,Shintaro Fukuhara,Shinichiro Fuse,Hiroyuki Nakamura
出处
期刊:Organic Letters
[American Chemical Society]
日期:2018-01-05
卷期号:20 (2): 433-436
被引量:35
标识
DOI:10.1021/acs.orglett.7b03760
摘要
Intramolecular electrophilic aromatic substitution (SEAr) reaction at the 5-position of isoxazoles was achieved. The electron-donating heteroatoms (N and O) at the 4-position of isoxazoles, which can be readily prepared based on our originally developed synthetic procedure, and a cationic gold(I) catalyst are essential for the intramolecular SEAr reaction to synthesize isoxazole-containing fused heterocycles. Structurally diverse isoxazolopyridines 6 and isoxazolopyrans 9, including base-labile 3-unsubstituted derivatives, were synthesized in good to high yields. The addition of N-phenylbenzaldimine as a hydrogen acceptor improved yields in the synthesis of isoxazolopyridines. Furthermore, synthesis of the tetracyclic fused ring system 12 was achieved by tandem cyclization from the corresponding diyne 11.
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