4.3 Article

Multistep microwave-assisted solvent-free organic reactions: Synthesis of 4-oxo-tetrahydro-pyridine

Journal

SYNTHETIC COMMUNICATIONS
Volume 34, Issue 2, Pages 345-359

Publisher

TAYLOR & FRANCIS INC
DOI: 10.1081/SCC-120027272

Keywords

microwave irradiation; 4-oxo-tetrahydro-pyridine; solvent-free; chirality; stereoselective synthesis

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Preparation and ring-closure of 2-dimethylaminomethylene-5-substituted-3-oxo-pent-4-enoic acid benzyl esters to dihydropyridine rings are efficiently and quickly carried out under solvent-free conditions in an open-vessel microwave system. The syntheses of 1,6-disubstituted-4-oxo-1,4,5,6-tetrahydro-pyridine-3-carboxylic acid benzyl esters are reported.

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