Synthesis of structurally diverse diarylketones through the diarylmethyl sp3 CH oxidation
摘要:
Under open-flask conditions, an efficient method to assemble a series of diversely functionalized diarylketones in the presence of commercially available NBS has been developed. Yields of up to 99% have been achieved employing diarylmethanes as starting material. Based on O-18-labeled experiment, the addition of stoichiometric water eventually leads to excellent yields in all carbonylation cases. (C) 2014 Elsevier Ltd. All rights reserved.
Decarboxylation with Carbon Monoxide: The Direct Conversion of Carboxylic Acids into Potent Acid Triflate Electrophiles
作者:R. Garrison Kinney、Bruce A. Arndtsen
DOI:10.1002/anie.201814660
日期:2019.4
carboxylic acids into potent acid triflate electrophiles. The reaction involves oxidative carbonylation of carboxylic acids with I2 in the presence of AgOTf, and is postulated to proceed via acyl hypoiodites that react with CO to form acid triflates. Coupling this chemistry with subsequent trapping with arenes offers a mild, room temperature approach to generate ketones directly from broadly available carboxylic
Lewis acid promoted electrophilic aromatic substitution reaction of nitrile oxide: Increase of the electrophilicity of carbon atom of nitrile oxide by Lewis acid complexation
作者:Jae Nyoung Kim、Eung K. Ryu
DOI:10.1016/s0040-4039(00)73637-9
日期:1993.5
Nitrile oxides complexed with Lewisacid have their increased electrophilic character at the carbon atom and could be used as hydroxynitrilium ion equivalents toward aromatic compounds.
与路易斯酸络合的腈氧化物在碳原子上具有增强的亲电子特性,可以用作芳族化合物的羟基腈离子当量。
Synthesis of (2-chlorophenyl)(phenyl)methanones and 2-(2-chlorophenyl)-1-phenylethanones by Friedel–Crafts acylation of 2-chlorobenzoic acids and 2-(2-chlorophenyl)acetic acids using microwave heating
作者:Jasia Mahdi、Haribabu Ankati、Jill Gregory、Brian Tenner、Edward R. Biehl
DOI:10.1016/j.tetlet.2011.03.052
日期:2011.5
Several 2-(2-chlorophenyl)-1-phenylethanones and (2-chlorophenyl)(phenyl)methanones were prepared by the Friedel-Crafts acylation reaction of 2-(2-chlorophenyl) acetic acids and 2-chlorocarboxylic acids, respectively, in the presence of cyanuric chloride, pyridine, and AlCl(3) or FeCl(3) using microwave heating. The yields of the ketones were significantly higher than those obtained using conventional heating. In addition, similar reactions carried out with the less inexpensive and less toxic FeCl(3) gave titled ketones in comparable yields. Interestingly, the FeCl(3) catalyzed reactions gave pure ketones (no chromatographic purification required), whereas the AlCl(3) catalyzed reaction gave impure product that required chromatographic purification. (C) 2011 Elsevier Ltd. All rights reserved.
Boron Trifluoride⋅Diethyl Ether-Catalyzed Etherification of Alcohols: A Metal-Free Pathway to Diphenylmethyl Ethers
A novel borontrifluoride⋅diethyl ether (BF3⋅OEt2)-catalyzed etherification procedure has been developed in which primary and secondary alcohols are easily converted into diphenylmethyl ethers with yields of up to 99%.
Under open-flask conditions, an efficient method to assemble a series of diversely functionalized diarylketones in the presence of commercially available NBS has been developed. Yields of up to 99% have been achieved employing diarylmethanes as starting material. Based on O-18-labeled experiment, the addition of stoichiometric water eventually leads to excellent yields in all carbonylation cases. (C) 2014 Elsevier Ltd. All rights reserved.