Cobalt-Mediated Macrocyclizations. Facile Synthesis of 2-Oxo Pyridinophanes via [2 + 2 + 2] Cycloaddition of α,ω-Diynes and Isocyanates
Organic Letters2003Vol. 5(24), pp. 4537–4540
Citations Over TimeTop 12% of 2003 papers
Abstract
[reaction: see text] Cobalt-mediated [2 + 2 + 2] cycloaddition of alpha,omega-diynes and isocyanates provides a direct approach to macrocyclic 2-oxopyridinophanes. This macrocyclization process, which proceeded most efficiently with aliphatic isocyanates, was conveniently performed at a moderate temperature (85 degrees C) without irradiation or syringe-pump addition.
Related Papers
- → Recent Progress in Metal-Catalyzed [2+2+2] Cycloaddition Reactions(2021)96 cited
- → Acetylene and Ethylene: Universal C2 Molecular Units in Cycloaddition Reactions(2021)27 cited
- → Addition Reactions: Cycloaddition(2017)1 cited
- → Addition Reactions: Cycloaddition(2019)
- → Addition Reactions: Cycloaddition(2014)