| Hui Yu, Associate Professor
School of Chemical Science and Engineering, Tongji University
|
Office:
| Engineering Test Center 221
Siping Road 1239, Shanghai 200092, P. R. China
|
Tel:
| +86-21-6598
|
Fax:
| +86-21-65981097
|
E-mail:
| yuhui@tongji.edu.cn
|
Introduction
Research interest:
1. Design and application of radical reactions in organic synthesis
2. Development of cross-dehydrogenative coupling reactions
Typical papers:
[1] Direct oxidative cross-coupling of toluene derivatives and N-acyl-2-aminoacetonphenones
*Yu, H.; Xu, Y.; Dong, R.; Fang, Y.Adv. Synth. Catal.2016, accepted
[2] Direct Synthesis of α-Alkoxy ketones by Oxidative C-O Bond Formation
*Yu, H.; Xu, Y.; Fang, Y.; Dong, R.Eur.J. Org. Chem.,2016, accepted
[3] Iron-Catalyzed Oxidative Coupling Reaction of N-Acyl Glycine Esters and Malonates
*Yu, H.; Liu, Z.; Lin, J. Synlett,2016, 27, 1711-1714
[4] NH4I-Catalyzed Synthesis of Sulfonamides from Arylsufonylhydrazides and Amines
*Yu, H.; Zhang, Y.Chin. J. Chem.2016,34, 359-362
[5] Dehydrogenative Cyclization of N-Acyl Dipeptide Esters for the Synthesis of Imidazolidin-4-ones
*Yu, H.; Shen, J. RSC Adv.,2015, 5, 9815-9818
[6] Copper-Catalyzed Synthesis of Imides from Aldehydes/Alcohols and Amine Hydrochloride Salts
*Yu, H.; Zhang, Y. Eur. J. Org. Chem.,2015, 1824-1828
[7] TBHP/TEMPO-Mediated Oxidative Synthesis of Imides from Amides
*Yu, H.; Chen, Y.; Zhang, Y.Chin. J. Chem.2015,33, 531-534
[8] Peroxidation of C−H Bonds Adjacent to an Amide Nitrogen Atom under Mild Conditions
*Yu, H.; Shen, J. Org. Lett.,2014, 16, 3204-3207
[9] TBHP/TBAI-Promoted Oxidative Cyclization of o-Acylphenols for the Construction of 2-Aryloxybenzofuran-3(2H)-ones
*Yu, H.; Zhang, F.; Huang, W. Synlett,2014, 25, 843-846
[10] Metal-Free Oxidative Cyclization of o-Acylphenols for the Construction of
2-Aminobenzofuran-3(2H)-ones
*Yu, H.; Huang, W.; Zhang, F. Eur. J. Org. Chem.,2014, 3156-3162
[11] Copper-Catalyzed Synthesis of Benzo[b]thiophenes and Benzothiazoles Using Thiocarboxylic Acids as a Coupling Partner
*Yu, H.; Zhang, M.; Li, Y. J. Org. Chem.,2013, 78, 8898-8903
