Publication | Closed Access
Dehydrogenative [2 + 2 + 2] Cycloaddition of Cyano-yne-allene Substrates: Convenient Access to 2,6-Naphthyridine Scaffolds
42
Citations
53
References
2015
Year
2,6-Naphthyridine DerivativesEngineeringHeterocyclic2,6-Naphthyridine ScaffoldsConvenient AccessCyano-yne-allene SubstratesOrganic ChemistryCatalysisChemistryCyano-yne-allene ScaffoldsUnsaturated Pyridine-containing CompoundsSynthetic ChemistryEnantioselective SynthesisBiomolecular Engineering
A rhodium-catalyzed [2 + 2 + 2] cycloaddition of cyano-yne-allene scaffolds followed by a dehydrogenative process enabling the direct synthesis of unsaturated pyridine-containing compounds that can be conveniently converted to 2,6-naphthyridine derivatives is reported.
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