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- Evaluation of P-bridged biaryl phosphine ligands in palladium-catalysed Suzuki–Miyaura cross-coupling reactions. Jairus L. Lamola, Paseka T. Moshapo, Cedric W. Holzapfel, Munaka Christopher Maumela
, RSC Adv.
, 2021
, 11
, 26883
- Molecular evolution pathways during nucleation of small organic molecules: solute-rich pre-nucleation species enable control over the nucleation process. Shuyi Zong, Jingkang Wang, Xin Huang, Ting Wang, Qi Liu, Beiqian Tian, Chuang Xie, Hongxun Hao
, Phys. Chem. Chem. Phys.
, 2020
, 22
, 18663
- 91. Homolytic aromatic substitution. Part XXVII. The reactions of toluene with some para-substituted diaroyl peroxides. J. K. Hambling, D. H. Hey, Gareth H. Williams
, J. Chem. Soc.
, 1962
, 487
- Microflow chemistry and its electrification for sustainable chemical manufacturing. Tai-Ying Chen, Yung Wei Hsiao, Montgomery Baker-Fales, Fabio Cameli, Panagiotis Dimitrakellis, Dionisios G. Vlachos
, Chem. Sci.
, 2022
, 13
, 10644
- Heterogenization of Pd–NHC complexes onto a silica support and their application in Suzuki–Miyaura coupling under batch and continuous flow conditions. Alberto Martínez, Jamin L. Krinsky, Itziar Peñafiel, Sergio Castillón, Konstantin Loponov, Alexei Lapkin, Cyril Godard, Carmen Claver
, Catal. Sci. Technol.
, 2015
, 5
, 310
- K-10 montmorillonite-catalyzed solid phase diazotizations: environmentally benign coupling of diazonium salts with aromatic hydrocarbons to biaryls. Garima Pandey, Béla Török
, Green Chem.
, 2017
, 19
, 5390
- A formal synthesis of both atropenantiomers of desertorin C. Rekha V. Kyasnoor, Melvyn V. Sargent
, Chem. Commun.
, 1998
, 2713
- The synthesis of desertorin C, a bicoumarin from the fungus Emericella desertorum. Mark A. Rizzacasa, Melvyn V. Sargent
, J. Chem. Soc., Perkin Trans. 1
, 1988
, 2425
- 259. Synthetical applications of activated metal catalysts. Part XII. The preparation of symmetrically substituted 2,2′-bipyridyls. W. H. F. Sasse, C. P. Whittle
, J. Chem. Soc.
, 1961
, 1347
- Reactions of lead tetra-acetate. Part XXI. Acyloxylation, plumbylation, and oxidative dimerisation of some benzenoid compounds in the presence of trifluoro- or trichloro-acetic acid. R. O. C. Norman, C. B. Thomas, J. S. Willson
, J. Chem. Soc. B
, 1971
, 518