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Search for "cyanobenzene" in Full Text gives 3 result(s) in Beilstein Journal of Organic Chemistry.
Photocatalysis with organic dyes: facile access to reactive intermediates for synthesis
Beilstein J. Org. Chem. 2020, 16, 1163–1187, doi:10.3762/bjoc.16.103
Synthesis and characterization of the cyanobenzene-ethylenedithio-TTF donor
Beilstein J. Org. Chem. 2015, 11, 951–956, doi:10.3762/bjoc.11.106
- Sandrina Oliveira Dulce Belo Isabel C. Santos Sandra Rabaca Manuel Almeida C²TN, Instituto Superior Técnico, Universidade de Lisboa, Estrada Nacional 10, P-2695-066 Bobadela LRS, Portugal 10.3762/bjoc.11.106 Abstract A dissymmetric TTF-type electron donor, cyanobenzene-ethylenedithio
- voltammetry, NMR, UV-visible and IR spectroscopy. Keywords: cross-coupling; cyanobenzene; cyclic voltammetry; dissymmetric tetrathiafulvalene; electro-active donors; Introduction The tetrathiafulvalene molecule (TTF) and its many derivatives, due to its unique π-donor properties, have been at the basis of
- report here a new non-symmetrically substituted TTF donor with one dithiin ring and one cyanobenzene ring obtained by a cross coupling reaction. These two rings are expected to enhance the degree of π-delocalization over the molecule when compared with simple TTF, while the presence of the nitrogen atom
Synthesis and physicochemical characterization of novel phenotypic probes targeting the nuclear factor-kappa B signaling pathway
Beilstein J. Org. Chem. 2013, 9, 900–907, doi:10.3762/bjoc.9.103
- against TNFα mediated NF-κB activation as measured in our reporter gene assay format. Probe 8 was synthesized as shown in Scheme 2 [12]. Reaction of 4-tert-butyl-cyanobenzene with hydroxylamine hydrochloride under microwave heating conditions resulted in the hydroxyamidine 6. This intermediate was
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