Consecutive nucleophilic substitution and aza Diels-Alder reaction - an efficient strategy to functionalized 2,2 '-bipyridines

Kozhevnikov, Dmitry N. and Kozhevnikov, Valery N. and Prokhorov, Anton M. and Ustinova, Maria M. and Rusinov, Vladimir L. and Chupakhin, Oleg N. and Aleksandrov, Grigory G. and Koenig, Burkhard (2006) Consecutive nucleophilic substitution and aza Diels-Alder reaction - an efficient strategy to functionalized 2,2 '-bipyridines. TETRAHEDRON LETTERS, 47 (6). pp. 869-872. ISSN 0040-4039,

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Abstract

An efficient strategy for the synthesis of functionalized 2,2'-bipyridines is reported. The strategy is based on readily available 3-pyridyl-1,2,4-triazine 4-oxides and uses a reaction sequence of nucleophilic substitution of hydrogen and aza Diels-Alder reaction. (c) 2005 Elsevier Ltd. All rights reserved.

Item Type: Article
Uncontrolled Keywords: COMPLEXES; PYRIDINE; LIGANDS; PHOTOPHYSICS; TERPYRIDINE; BIPYRIDINE; CHEMISTRY; CRYSTAL; FACILE;
Subjects: 500 Science > 540 Chemistry & allied sciences
Divisions: Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König
Depositing User: Dr. Gernot Deinzer
Date Deposited: 23 Feb 2021 12:12
Last Modified: 23 Feb 2021 12:12
URI: https://pred.uni-regensburg.de/id/eprint/34947

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