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Synth Commun. 2011;41(7):2615-2623. Epub 2011 Jun 29.

SYNTHESIS OF N-SUBSTITUTED CARBONYLAMINO-1,2,3,6-TETRAHYDROPYRIDINES AS POTENTIAL ANTI-INFLAMMATORY AGENTS.

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1
College of Pharmacy and Pharmaceutical Sciences, Florida A&M University, Tallahassee, Florida, USA.

Abstract

Several N-substituted carbonyl/sulfonylamino-1,2,3,6-tetrahydropyridines (5a-i and 9a, b) were synthesized via sodium borohydride reduction of the corresponding N-substitutedimino-pyridinium ylides (4a-i and 8a, b) in absolute ethanol.

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