Results
1 -
10 of
10
(Click
here to explore results)
Enabling room-temperature reductive C–N coupling of nitroarenes: combining homogeneous and heterogeneous synergetic catalyses mediated by light . Xuexue Dong, Yiying Yang, Yang Shen, Aihua Yuan, Zengjing Guo, Heng Song, Fu Yang
, Green Chem.
, 2022
, 24
, 4012
Full theoretical protocol for the design of metal-free organic electron donor–spacer–acceptor systems . Amílcar Duque-Prata, Carlos Serpa, Pedro J. S. B. Caridade
, Phys. Chem. Chem. Phys.
, 2023
, 25
, 27854
Nucleophilic strategies to construct –CF2 – linkages using borazine-CF2 Ar reagents . Michael M. Wade Wolfe, Shuo Guo, Lucy S. Yu, Trenton R. Vogel, Joseph W. Tucker, Nathaniel K. Szymczak
, Chem. Commun.
, 2022
, 58
, 11705
Facile synthesis of hexagonal α-Co(OH)2 nanosheets and their superior activity in the selective reduction of nitro compounds . Jiahui Guo, Xueqing Feng, Songrui Wang, Qikang Wu, Shanshan Lv, Yan Zhou, Han Li, Zheng Chen, Yuzhong Zhang
, Dalton Trans.
, 2021
, 50
, 18061
Efficient and highly selective iron-catalyzed reduction of nitroarenes . Rajenahally V. Jagadeesh, Gerrit Wienhöfer, Felix A. Westerhaus, Annette-Enrica Surkus, Marga-Martina Pohl, Henrik Junge, Kathrin Junge, Matthias Beller
, Chem. Commun.
, 2011
, 47
, 10972
The synthesis of certain trifluoromethylquinoline derivatives . R. Belcher, M. Stacey, A. Sykes, J. C. Tatlow
, J. Chem. Soc.
, 1954
, 3846
Notes . W. Gerrard, W. J. Green, R. A. Nutkins, A. Sykes, J. C. Tatlow, C. C. Addison, J. Lewis, R. L. Jones, R. J. W. Le Fèvre, J. Northcott, R. H. Hall, E. S. Stern, J. R. Naylor, A. M. Islam, R. A. Raphael
, J. Chem. Soc.
, 1952
, 4076
Further investigations of trifluoromethyldiphenyl derivatives . M. R. Pettit, J. C. Tatlow
, J. Chem. Soc.
, 1954
, 1071
587. The synthesis of some perfluoroalkylbenzimidazoles . B. C. Bishop, A. S. Jones, J. C. Tatlow
, J. Chem. Soc.
, 1964
, 3076
The direct trifluoromethylation of aryl chlorides using Burton's reagent . James H. Clark, Martin A. McClinton, Robert J. Blade
, J. Chem. Soc., Chem. Commun.
, 1988
, 638