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Revision of the stereochemistry of the reductive Heck cyclisation of 1-(2-iodobenzoyl)-4-substituted-1.4-dihydro-pyridine-3-carbaldehyde aminals
Authors:Pierre Mangeney  Christophe Pays
Institution:Laboratoire de Chimie Organique, UMR 7611 Université P. et M. Curie, 4 place Jussieu, F-75252 Paris cedex 05, France
Abstract:The stereochemistry of reductive and non reductive Heck cyclisations of 4-substituted-1.4-dihydropyridines is reexamined. The both reactions occur mainly via an anti (from the C4 substituent) 5-exo process without any epimerisation of the C4-H.
Keywords:dihydropyridines  chiral aminals  Heck reactions  isondolone synthesis
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