Hafnium Triflate as an Efficient Catalyst for Direct Friedel-Crafts Reactions of Chromene Hemiacetals

被引:36
|
作者
Wu, Yan-Chao [1 ]
Li, Hui-Jing [1 ]
Liu, Li [1 ]
Demoulin, Nicolas [2 ]
Liu, Zhe [1 ]
Wang, Dong [1 ]
Chen, Yong-Jun [1 ]
机构
[1] Chinese Acad Sci, Inst Chem, BNLMS, CAS Key Lab Mol Recognit & Funct, Beijing 100190, Peoples R China
[2] CNRS, Inst Chim Subst Nat, F-91198 Gif Sur Yvette, France
基金
中国国家自然科学基金;
关键词
chromenes; Friedel-Crafts reaction; hafnium; hemiacetals; selectivity; ELECTRON-RICH ARENES; ASYMMETRIC-SYNTHESIS; ALLYLIC ALKYLATION; ENANTIOSELECTIVE SYNTHESIS; MULTICOMPONENT APPROACH; SALICYLIC ALDEHYDES; FACILE SYNTHESIS; ALCOHOLS; GLYCOSYLATION; AMINOMETHYLATION;
D O I
10.1002/adsc.201000930
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The direct Friedel-Crafts reaction of chromene hemiacetals with indoles, furans and sterically hindered anilines has been accomplished with high selectivity and excellent yields in the presence of a catalytic amount of hafnium triflate [Hf(OTf)(4), 0.1 mol%, 0-40 degrees C]. The mild conditions tolerate various sensitive functional and protecting groups, and the products were confirmed unambiguously from their spectra and by single-crystal X-ray analysis. This direct Friedel-Crafts reaction of chromene hemiacetals should inspire and encourage the consideration of hafnium triflate in the development of mild reaction conditions for the efficient derivatization of hemiacetal-containing compounds.
引用
收藏
页码:907 / 912
页数:6
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