389614-52-2Relevant academic research and scientific papers
Hypervalent iodine(iii) sulfonate mediated synthesis of 6-arylimidazo[2,1-b]thiazoles in liquid PEG-400
Wu, Fang-Wen,Hou, Rei-Sheu,Wang, Huey-Min,Kang, Iou-Jiun,Chen, Ling-Ching
experimental part, p. 663 - 666 (2012/07/03)
PEG-400[poly(ethylene glycol-400)] is used as reaction medium in the one-pot synthesis of 6-arylimidazo[ 2,1-b]thiazoles by reaction with aryl ketones, hypervalent iodine(III) sulfonate and 2-aminothiazole. Significant rate enhancements and improved yield
Hypervalent iodine(III) sulfonate mediated synthesis of 2-arylimidazo[1,2-a]pyrimidines in liquid PEG-400
Cheng, Hui-Ting,Hou, Rei-Sheu,Wang, Huey-Min,Kang, Iou-Jiun,Lin, Pei-Ying,Chena, Ling-Ching
experimental part, p. 632 - 635 (2010/06/13)
PEG-400[poly(ethylene glycol-400)] is used as a "green" recyclable solvent in the one-pot synthesis of 2-arylimidazo[1,2-a]pyrimidines by reaction with ketones, [hydroxyl(2,4-dinitrobenzenesulfonyloxy)-iodo]benzene (HDNIB), and 2-aminopyrimidine. Signific
Hypervalent iodine(iii) sulfonate mediated synthesis of quinoxalines in liquid peg-400
Lin, Pei-Ying,Hou, Rei-Sheu,Wang, Huey-Min,Kang, Iou-Jiun,Chen, Ling-Ching
experimental part, p. 683 - 687 (2010/08/13)
PEG-400[poly(ethylene glycol-400)] is used as a "green" recyclable solvent in the one-pot synthesis of quinoxalines by reaction with aryl ketones, hypervalent Iodine(III) Sulfonate, and o-phenylenediamines. Significant rate enhancements and improved yields have been observed.
Hypervalent lodine(III) sulfonate reagent mediated synthesis of 4-aryl-2-phenyloxazoles in ionic liquid
Cheng, Hui-Ting,Hou, Rei-Sheu,Wang, Huey-Min,Chen, Ling-Ching
experimental part, p. 919 - 922 (2009/12/04)
A new and efficient method for the synthesis of 4-aryl-2-phenyloxazoles is described which is based upon the reaction of α-[(2,4-dinitrobenzene) sulfonyl]oxy ketone intermediates with benzamide in ionic liquid.
Efficient Conversion of Alkyl Aryl Ketones to Aromatic Carboxylic Acids
Lee, Jong Chan,Choi, Ju-Hee,Lee, Yong Chan
, p. 1563 - 1564 (2007/10/03)
An efficient method for the conversion of alkyl aryl ketones to aromatic carboxylic acids has been developed based on initial formation of α-organosulfonyloxy ketones and their subsequent oxidation reactions by tetrabutylammonium periodate in one-pot conditions.
