75526-18-0Relevant articles and documents
Divergent Palladium-Catalyzed Tandem Reaction of Cyanomethyl Benzoates with Arylboronic Acids: Synthesis of Oxazoles and Isocoumarins
Chen, Jiuxi,Chen, Zhongyan,Dai, Ling,Shao, Yinlin,Xiong, Wenzhang,Xu, Tong,Yu, Shuling
supporting information, (2020/04/15)
A palladium-catalyzed tandem reaction of cyanomethyl benzoates with arylboronic acids has been achieved. Substitution at the 2-position of cyanomethyl benzoates was found to be crucial for the selective synthesis of oxazoles and isocoumarins. Cyanomethyl
A novel synthetic method of 2,4-disubstituted oxazoles using carboxylic acid-derived Bu2Sn[OC(O)R]2
Yoneyama, Hiroki,Oka, Naoki,Usami, Yoshihide,Harusawa, Shinya
, (2020/05/21)
A novel synthetic method for the preparation of 2,4-disubstituted oxazoles was developed, entailing the reaction of dibutyltin diacylates Bu2Sn[OC(O)R]2 with 1-substituted acetylenes and TMSN3 to afford a range of 2,4-disu
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.
Suzuki coupling of oxazoles
Flegeau, Emmanuel Ferrer,Popkin, Matthew E.,Greaney, Michael F.
, p. 2495 - 2498 (2007/10/03)
A protocol for the functionalization of the oxazole 2- and 4-positions using the Suzuki coupling reaction is described. 2-Aryl-4-trifloyloxazoles undergo rapid, microwave-assisted coupling with a range of aryl and heteroaryl boronic acids in good to excel
