Synthesis of four new carboxylic derivatives based on the [1.1.1.1]metacyclophane backbone blocked in 1,3-Alternate conformation |
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Authors: | Ekaterina F. Chernova Alexander S. Ovsyannikov Sylvie Ferlay Svetlana E. Solovieva Igor S. Antipin Alexander I. Konovalov Nathalie Kyritsakas Mir Wais Hosseini |
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Affiliation: | 1. Molecular Tectonics Laboratory, University of Strasbourg, UMR UDS–CNRS 7140, Institut le Bel, 4, Rue Blaise Pascal, F-67000 Strasbourg, France;2. Kazan Federal University, Kremlevskaya Str.18, 420008 Kazan, Russian Federation;3. A.E. Arbuzov Institut of Organic and Physical Chemistry of Kazan Scientific Center of Russian Academy of Science, Arbuzov Str. 8., 420008 Kazan, Russian Federation |
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Abstract: | Four new tetrasubstituted [1.1.1.1]metacyclophanes (4–7), that are inherently adopting a 1,3-Alternate conformation, bearing four or eight peripheral carboxylic binding sites, and appended with spacers group (alkyl or phenyl) differing by the flexibility, have been synthesised in high yields. The structures of the obtained compounds have been investigated in solution as well as in the solid state, for three of them, by using single-crystal X-ray analysis. |
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Keywords: | Carboxylate ligand 1,3-Alternate conformation Metacyclophane backbone Ester derivatives Suzuki coupling |
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