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- Paired electrochemical C–H bromination of (hetero)arenes with 2-bromoethan-1-ol. Yanxia Lv, Zhong-Wei Hou, Pinhua Li, Lei Wang
, Org. Chem. Front.
, 2023
, 10
, 990
- Eco-friendly preparation of ultrathin biomass-derived Ni3S2-doped carbon nanosheets for selective hydrogenolysis of lignin model compounds in the absence of hydrogen. Changzhou Chen, Dichao Wu, Peng Liu, Jing Li, Haihong Xia, Minghao Zhou, Jianchun Jiang
, Green Chem.
, 2021
, 23
, 3090
- Hydrophobic species-enabled acid–base multi-catalysis for stereoselective access to renewable trans-anethole. Yixuan Liu, Mingrui Li, Tengyu Liu, Jinyu Tan, Samuel Lalthazuala Rokhum, Heng Zhang, Song Yang, Hu Li
, Dalton Trans.
, 2022
, 51
, 16668
- Natural benzofurans. Synthesis of eupomatenoids-1, -3, -4, -5, -6, -7, and -13. Brian A. McKittrick, Robert Stevenson
, J. Chem. Soc., Perkin Trans. 1
, 1983
, 475
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Ruthenium-catalyzed redox isomerization/transfer hydrogenation in organic and aqueous media: A one-pot tandem process for the reduction of allylic alcohols. Victorio Cadierno, Pascale Crochet, Javier Francos, Sergio E. García-Garrido, José Gimeno, Noel Nebra
, Green Chem.
, 2009
, 11
, 1992
- The chemistry of fungi. Part LXXII. The trimethylsilyloxy-substituent as a leaving group. John M. Midgley, Jeffrey S. Millership, W. Basil Whalley
, J. Chem. Soc., Perkin Trans. 1
, 1976
, 1384
- Some observations on the double layer capacity at mercury electrodes. I. M. Barclay, J. A. V. Butler
, Trans. Faraday Soc.
, 1940
, 35
, 128
- Ruthenium-catalyzed reduction of allylic alcohols: An efficient isomerization/transfer hydrogenation tandem process. Victorio Cadierno, Javier Francos, José Gimeno, Noel Nebra
, Chem. Commun.
, 2007
, 2536
- Synthesis and characterization of novel solid–solid phase change materials with a polyurethaneurea copolymer structure for thermal energy storage. Changzhong Chen, Wenmin Liu, Hongwei Wang, Lanlan Zhu
, RSC Adv.
, 2016
, 6
, 102997
- Geometrical isomerism of the azonaphthalenes. Max Frankel, Reuven Wolovsky, Ernst Fischer
, J. Chem. Soc.
, 1955
, 3441