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Synthesis of 1,4-Dihydropyridines by Regioselective Additions of Benzylic Zinc Bromides to Pyridinium Salts and Their Aromatizations to 4-Benzylpyridines
14
Citations
29
References
1997
Year
Chemical EngineeringEngineeringHeterocyclicHigh RegioselectivityOrganic ChemistryRegioselective AdditionsBenzylic Zinc BromidesDecalin AffordSynthetic ChemistryChemistryHeterocycle ChemistrySynthesis MethodPyridinium SaltsMethyl Nicotinate
Abstract Benzylic zinc reagents add with high regioselectivity to 1-(phenoxycarbonyl) salts of methyl nicotinate to yield methyl-1-(phenoxylcarbonyl)-4-benzyl-1,4-dihydronicotinates. The dihydronicotinates on heating with sulfur in decalin afford methyl 4-benzylnicotinates.
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