A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines-Reference-Cited by-同舟云学术

A Direct Route to 6,6’-Disubstituted-2,2’-Bipyridines by Double Diels-Alder/retro Diels-Alder Reaction of 5,5’-bi-1,2,4-Triazines

Published:2005-01-31 Issue:1 Volume:10 Page:274-278
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Branowska D.

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/10/1/274/pdf

Reference22 articles.

1. Synthesis of Unsymmetrical Annulated 2,2’-Bipyridine Analogues with Attached Cycloalkene and Piperidine Rings via Sequential Diels-Alder Reaction of 5,5’-bi-1,2,4-triazines

2. Supramolecular Chemistry: Concepts and Perspectives;Lehn

3. Bipyridine: The Most Widely Used Ligand. A Review of Molecules Comprising at Least Two 2,2‘-Bipyridine Units

4. The Ullmann Synthesis of Biaryls

5. Synthesis of 2,2′‐Bipyridines: Versatile Building Blocks for Sexy Architectures and Functional Nanomaterials

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5. Synthesis of unsymmetric 6,6´-diaryl-2,2´-bipyridines using a 1,2,4-triazine methodology;Russian Chemical Bulletin;2015-03