Publication | Closed Access
Cobalt-Mediated Macrocyclizations. Facile Synthesis of 2-Oxo Pyridinophanes via [2 + 2 + 2] Cycloaddition of α,ω-Diynes and Isocyanates
42
Citations
10
References
2003
Year
Macrocyclization ProcessChemical EngineeringEngineeringHeterocyclicBiochemistryModerate TemperatureNatural SciencesFacile SynthesisDiversity-oriented Synthesis2-Oxo PyridinophanesCobalt-mediated MacrocyclizationsOrganic ChemistrySyringe-pump AdditionCatalysisOrganometallic CatalysisChemistryHeterocycle ChemistrySynthetic Chemistry
[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.
| Year | Citations | |
|---|---|---|
Page 1
Page 1