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

Kozhevnikov, Dmitry N., Kozhevnikov, Valery N., Prokhorov, Anton M., Ustinova, Maria M., Rusinov, Vladimir L., Chupakhin, Oleg N., 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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Date of publication of this fulltext: 05 Aug 2009 13:21

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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.


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Item type:Article
Date:9 February 2006
Institutions:Chemistry and Pharmacy > Institut für Organische Chemie > Lehrstuhl Prof. Dr. Burkhard König
Identification Number:
ValueType
10.1016/j.tetlet.2005.12.006DOI
Dewey Decimal Classification:500 Science > 540 Chemistry & allied sciences
Status:Published
Refereed:Yes, this version has been refereed
Created at the University of Regensburg:Partially
Item ID:46
Owner only: item control page

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