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- Nickel-catalyzed cross-electrophile coupling of aryl chlorides with allylic alcohols. Hang Yu, Zhong-Xia Wang
, Org. Biomol. Chem.
, 2021
, 19
, 9723
- The bulky Pd-PEPPSI-embedded conjugated microporous polymer-catalyzed Suzuki–Miyaura cross-coupling of aryl chlorides and arylboronic acids. Chang-An Wang, Wei Zhao, Yan-Wei Li, Yin-Feng Han, Jian-Ping Zhang, Qun Li, Kun Nie, Jian-Guo Chang, Feng-Shou Liu
, Polym. Chem.
, 2022
, 13
, 1547
- Methanolysis (solvolysis) and synthesis of 4′-substituted 4-benzyloxybenzyl chlorides and some related compounds: comparisons with the corresponding benzoyl compounds. Jorge Armando Luis Jorge, Nilo Zengo Kiyan, Yukino Miyata, Joseph Miller
, J. Chem. Soc., Perkin Trans. 2
, 1981
, 100
- New access to (η5-cyclohexadienyl)Mn(CO)3 and cationic (η6-arene)Mn(CO)3 complexes by Suzuki–Miyaura reaction. Françoise Rose-Munch, Alex Marti, Derya Cetiner, Jean-Philippe Tranchier, Eric Rose
, Dalton Trans.
, 2011
, 40
, 1567
- Reactions of lead tetra-acetate. Part XIII. Homolytic and heterolytic mechanisms in the oxidation of alcohols. R. O. C. Norman, R. A. Watson
, J. Chem. Soc. B
, 1968
, 692
- Bu3SnH mediated oxidative radical cyclisations: synthesis of 6H-benzo[c]chromen-6-ones . W. Russell Bowman, Emma Mann, Jonathan Parr
, J. Chem. Soc., Perkin Trans. 1
, 2000
, 2991
- Iodine-catalyzed disproportionation of aryl-substituted ethers under solvent-free reaction conditions. Marjan Jereb, Dejan Vražič
, Org. Biomol. Chem.
, 2013
, 11
, 1978
- Highly regioselective C–H bond functionalization: palladium-catalyzed arylation of substituted imidazo[1,2-a]pyridine with aryl chlorides. Hua Cao, Yuanguang Lin, Haiying Zhan, Zuodong Du, Xiulian Lin, Qi-Mei Liang, Hong Zhang
, RSC Adv.
, 2012
, 2
, 5972
- Cobalt-catalyzed carboxylation of aryl and vinyl chlorides with CO2. Yanwei Wang, Xiaomei Jiang, Baiquan Wang
, Chem. Commun.
, 2020
, 56
, 14416
- Synthesis and characterization of trinuclear N-heterocyclic carbene–palladium(ii) complexes and their applications in the Suzuki–Miyaura cross-coupling reaction. Tao Wang, Lantao Liu, Kai Xu, Huanping Xie, Hui Shen, Wen-Xian Zhao
, RSC Adv.
, 2016
, 6
, 100690