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Hafnium Triflate as an Efficient Catalyst for Direct Friedel–Crafts Reactions of Chromene Hemiacetals
Author(s) -
Wu YanChao,
Li HuiJing,
Liu Li,
Demoulin Nicolas,
Liu Zhe,
Wang Dong,
Chen YongJun
Publication year - 2011
Publication title -
advanced synthesis and catalysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.541
H-Index - 155
eISSN - 1615-4169
pISSN - 1615-4150
DOI - 10.1002/adsc.201000930
Subject(s) - friedel–crafts reaction , chemistry , trifluoromethanesulfonate , hafnium , hemiacetal , derivatization , catalysis , steric effects , selectivity , reagent , chemoselectivity , combinatorial chemistry , organic chemistry , high performance liquid chromatography , zirconium
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 °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.

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