A Short Synthetic Route to 4,7‐Dihalogenated 1,10‐Phenanthrolines with Additional Groups in 3,8‐Position: Soluble Precursors for Macrocyclic Oligophenanthrolines
Author:
Affiliation:
1. Institut für Organische Chemie der Universität Würzburg, Am Hubland, D‐97074 Würzburg, Fax: (internat.) +49(0)931/888‐4606
Publisher
Wiley
Subject
Organic Chemistry,Physical and Theoretical Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/%28SICI%291099-0690%28199805%291998%3A5%3C785%3A%3AAID-EJOC785%3E3.0.CO%3B2-%23
Reference40 articles.
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2. Optically active phenanthrolines in asymmetric catalysis
3. Optically active phenanthrolines in asymmetric catalysis. III. Highly efficient enantioselective transfer hydrogenation of acetophenone by chiral rhodium/3-alkyl phenanthroline catalysts.
4. Photochemical reduction of carbon dioxide to formate catalyzed by 2,2t́-bipyridine- or 1,10-phenanthroline-ruthenium(II) complexes
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