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- Direct transformation of benzyl esters into esters, amides, and anhydrides using catalytic ferric(iii) chloride under mild conditions. Van Hieu Tran, Truong Giang Luu, Anh Thu Nguyen, Hee-Kwon Kim
, Org. Biomol. Chem.
, 2023
, 21
, 8494
- Gas-phase preparation of azulene (C10H8) and naphthalene (C10H8) via the reaction of the resonantly stabilized fulvenallenyl (C7H5˙) and propargyl (C3H3˙) radicals. Wang Li, Jiuzhong Yang, Long Zhao, David Couch, Myrsini San Marchi, Nils Hansen, Alexander N. Morozov, Alexander M. Mebel, Ralf I. Kaiser
, Chem. Sci.
, 2023
, 14
, 9795
- Electrolysis of trichloromethylated organic compounds under aerobic conditions catalyzed by the B12 model complex for ester and amide formation. Hisashi Shimakoshi, Zhongli Luo, Takuya Inaba, Yoshio Hisaeda
, Dalton Trans.
, 2016
, 45
, 10173
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Reductive electron transfer on trichloromethyl derivatives of benzene
and pyridine studied by electrochemical methods
. Marco Borsari, Daniela Dallari, Claudio Fontanesi, Giovanna Gavioli, Dario Iarossi, Roberta Piva, Ferdinando Taddei
, J. Chem. Soc., Perkin Trans. 2
, 1997
, 1839
- Convenient synthesis of aromatic acid chlorides. The reaction of benzylidyne chlorides with hexamethyldisiloxane. Taichi Nakano, Kazuhiro Ohkawa, Hideyuki Matsumoto, Yoichiro Nagai
, J. Chem. Soc., Chem. Commun.
, 1977
, 808b
- Serendipitous discoveries of new coordination modes of the 1,5-regioisomer of 1,2,3-triazoles enroute to the attempted synthesis of a carbon-anchored tri-mesoionic carbene. Lisa Suntrup, Merlin Kleoff, Biprajit Sarkar
, Dalton Trans.
, 2018
, 47
, 7992
- Theoretical MO ab initio investigation of the reductive C–Cl bond cleavage in benzyl chloride, benzotrichloride † and in the analogous 4-pyridine derivatives. Rois Benassi, Claudio Bertarini, Ferdinando Taddei
, J. Chem. Soc., Perkin Trans. 2
, 1997
, 2263
- A flexible Pinner preparation of orthoesters: the model case of trimethylorthobenzoate. Marco Noè, Alvise Perosa, Maurizio Selva
, Green Chem.
, 2013
, 15
, 2252
- Photochlorination of toluene – the thin line between intensification and selectivity. Part 1: intensification and effect of operation conditions. Ümit Taştan, Dirk Ziegenbalg
, React. Chem. Eng.
, 2021
, 6
, 82
- Molecular polarisability. Hyperconjugative effects in t-butylbenzene and in benzotrichloride. M. J. Aroney, K. E. Calderbank, R. J. W. Le Fèvre, R. K. Pierens
, J. Chem. Soc. B
, 1970
, 1120