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- Spin trapping of superoxide by diester-nitrones. Ahmad Allouch, Valérie Roubaud, Robert Lauricella, Jean-Claude Bouteiller, Béatrice Tuccio
, Org. Biomol. Chem.
, 2005
, 3
, 2458
- Computational design of an imine reductase: mechanism-guided stereoselectivity reversion and interface stabilization. Kai Wu, Jinrong Yan, Qinde Liu, Xiaojing Wang, Piaoru Wu, Yiyang Cao, Xiuhong Lu, Yixin Xu, Junhai Huang, Lei Shao
, Chem. Sci.
, 2024
, 15
, 1431
- Cationic Rh and Ir complexes containing bidentate imidazolylidene–1,2,3-triazole donor ligands: synthesis and preliminary catalytic studies. Khuong Q. Vuong, Marina G. Timerbulatova, Matthew B. Peterson, Mohan Bhadbhade, Barbara A. Messerle
, Dalton Trans.
, 2013
, 42
, 14298
- Asymmetric synthesis of chiral cyclic amine from cyclic imine by bacterial whole-cell catalyst of enantioselective imine reductase. Koichi Mitsukura, Mai Suzuki, Kazuhiro Tada, Toyokazu Yoshida, Toru Nagasawa
, Org. Biomol. Chem.
, 2010
, 8
, 4533
- Metal-mediated synthesis of pyrrolines. Noelia S. Medran, Agustina La-Venia, Sebastian A. Testero
, RSC Adv.
, 2019
, 9
, 6804
- Improvement of (S)-selective imine reductase GF3546 for the synthesis of chiral cyclic amines. Yuta Fukawa, Keita Yoshida, Sayaka Degura, Koichi Mitsukura, Toyokazu Yoshida
, Chem. Commun.
, 2022
, 58
, 13222
- ESR study of the spin adducts of three analogues of DEPMPO substituted at C4 or C3. Florence Chalier, Jean-Louis Clément, Micaël Hardy, Paul Tordo, Antal Rockenbauer
, RSC Adv.
, 2014
, 4
, 11610
- Enantioselective imine reduction catalyzed by imine reductases and artificial metalloenzymes. Daniela Gamenara, Pablo Domínguez de María
, Org. Biomol. Chem.
, 2014
, 12
, 2989
- Recent progress in anion exchange membranes (AEMs) in water electrolysis: synthesis, physio-chemical analysis, properties, and applications. Ganesan Sriram, Karmegam Dhanabalan, Kanalli V. Ajeya, Kanakaraj Aruchamy, Yern Chee Ching, Tae Hwan Oh, Ho-Young Jung, Mahaveer Kurkuri
, J. Mater. Chem. A
, 2023
, 11
, 20886
- Studies in the pyrroline series. Part VI. The formulation of the base C13H23NO3 as a 1-pyrroline 1-oxide. Franco Agolini, R. Bonnett, D. E. McGreer, G. F. Stephenson
, J. Chem. Soc. C
, 1966
, 1491