One-Pot Domino Synthesis of Polyfunctionalized Benzophenones, Dihydroxanthones, and m-Terphenyls from 2-(Polyfluoroalkyl)chromones

被引:10
作者
Sosnovskikh, Vyacheslav Ya [1 ]
Korotaev, Vladislav Yu [1 ]
Barkov, Alexey Yu [1 ]
Kutyashev, Igor B. [1 ]
Safrygin, Alexander V. [1 ]
机构
[1] Ural Fed Univ, Inst Nat Sci, Dept Chem, Ekaterinburg 620000, Russia
基金
俄罗斯基础研究基金会;
关键词
Domino reactions; Molecular diversity; Fluorine; Arenes; VINYLOGOUS ALDOL REACTION; MICHAEL ADDITION; 2-POLYFLUOROALKYLCHROMONES; DERIVATIVES; INHIBITORS; MALONONITRILES; REARRANGEMENT; EQUIVALENT; CHEMISTRY; KETONES;
D O I
10.1002/ejoc.201403585
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Whereas 2-(polyfluoroalkyl)chromones activated by electron-withdrawing substituents in the benzene ring react with 2-(1-phenylalkylidene)malononitriles in the presence of triethylamine in dichloromethane to produce a wide range of polyfunctionalized benzophenones and dihydroxanthones, their reactions with ethyl -cyano--methylcinnamate under the same conditions took an entirely different course and gave mainly m-terphenyl derivatives. The difference in behavior between the ylidene derivatives of malononitrile and those of ethyl cyanoacetate is remarkable.
引用
收藏
页码:1932 / 1944
页数:13
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