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- Homogeneously-catalysed hydrogen release/storage using the 2-methylindole/2-methylindoline LOHC system in molten salt-organic biphasic reaction systems. Alexander Søgaard, Marlene Scheuermeyer, Andreas Bösmann, Peter Wasserscheid, Anders Riisager
, Chem. Commun.
, 2019
, 55
, 2046
- Highly efficient red fluorescent dyes for organic light-emitting diodes. Yuan Jay Chang, Tahsin J. Chow
, J. Mater. Chem.
, 2011
, 21
, 3091
- Asymmetric C(sp3)-H/C(Ar) coupling reactions. Highly enantio-enriched indolines via regiodivergent reaction of a racemic mixture. Dmitry Katayev, Masafumi Nakanishi, Thomas Bürgi, E. Peter Kündig
, Chem. Sci.
, 2012
, 3
, 1422
- Mononuclear complexes of a tridentate redox-active ligand with sulfonamido groups: structure, properties, and reactivity. Sarah A. Cook, Justin A. Bogart, Noam Levi, Andrew C. Weitz, Curtis Moore, Arnold L. Rheingold, Joseph W. Ziller, Michael P. Hendrich, A. S. Borovik
, Chem. Sci.
, 2018
, 9
, 6540
- Kinetic resolution of (±)-2-methyl-1,2,3,4-tetrahydroquinoline and (±)-2-methylindoline. Victor P. Krasnov, Galina L. Levit, Irina N. Andreeva, Alexander N. Grishakov, Valerii N. Charushin, Oleg N. Chupakhin
, Mendeleev Commun.
, 2002
, 12
, 27
- Homogeneous palladium-catalyzed asymmetric hydrogenation. Qing-An Chen, Zhi-Shi Ye, Ying Duan, Yong-Gui Zhou
, Chem. Soc. Rev.
, 2013
, 42
, 497
- Homogeneous catalysis with polyhydride complexes. Juan C. Babón, Miguel A. Esteruelas, Ana M. López
, Chem. Soc. Rev.
, 2022
, 51
, 9717
- Visible light-responsive materials: the (photo)chemistry and applications of donor–acceptor Stenhouse adducts in polymer science. Michèle Clerc, Sara Sandlass, Omar Rifaie-Graham, Julie A. Peterson, Nico Bruns, Javier Read de Alaniz, Luciano F. Boesel
, Chem. Soc. Rev.
, 2023
, 52
, 8245
- Synthesis of quinoxalinones by the reaction of o-phenylenediamines with dimethyl acetylenedicarboxylate. Hans Suschitzky, Basil J. Wakefield, Roger A. Whittaker
, J. Chem. Soc., Perkin Trans. 1
, 1975
, 401
- Conversion of amines into imines by swern oxidation. David Keirs, Karl Overton
, J. Chem. Soc., Chem. Commun.
, 1987
, 1660