Consecutive nucleophilic substitution and aza Diels–Alder reaction—an efficient strategy to functionalized 2,2′-bipyridines-Reference-Cited by-同舟云学术

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

Published:2006-02 Issue:6 Volume:47 Page:869-872
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Kozhevnikov Dmitry N.,Kozhevnikov Valery N.,Prokhorov Anton M.,Ustinova Maria M.,Rusinov Vladimir L.,Chupakhin Oleg N.,Aleksandrov Grigory G.,König Burkhard

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference23 articles.

1. Chiral 2,2‘-Bipyridines, 1,10-Phenanthrolines, and 2,2‘:6‘,2‘ ‘-Terpyridines: Syntheses and Applications in Asymmetric Homogeneous Catalysis

2. Photosensitization and Photocatalysis Using Inorganic and Organic Compounds;Ziessel,1993

3. Determination of Fe(II) and total iron in natural waters with 3-(2-pyridyl)-5,6-diphenyl-1,2,4-triazine (PDT)

4. SELECTIVE EXTRACTION OF Am(III) OVER Eu(III) BY 2,6-DITRIAZOLYL- AND 2,6-DITRIAZINYLPYRIDINES1

5. Synthesis and Fluorescence Properties of Manisyl-Substituted Terpyridine, Bipyridine, and Phenanthroline

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