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 König, 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.

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Other URL: http://dx.doi.org/10.1016/j.tetlet.2005.12.006

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.

Item Type:Article
Institutions: Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König
Identification Number:
ValueType
10.1016/j.tetlet.2005.12.006DOI
Subjects:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Partially
Owner:Regina Hoheisel
Deposited On:05 Jul 2006
Last Modified:20 Jul 2011 22:47
Item ID:46
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