Stereoselective synthesis of 3,4-disubstituted and 3,4,5-trisubstituted piperidiens by Lewis acid-catalysed ene cyclisation of 4-aza-1,7-dienes

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Authors

Colleges, School and Institutes

Abstract

The thermal or Lewis acid-catalysed ene cyclisation of a variety of 4-aza-1,7-dienes afforded 3,4-disubstituted or 3,4,5-trisubstituted piperidines. Activation of the enophile with a single ester facilitated a thermal ene cyclisation, although the reaction was not amenable to Lewis acid catalysis. With other activating groups on the enophile it was found that Lewis acid catalysis was facile, although there was a. ne balance between the desired ene cyclisation and the competing hetero-Diels-Alder reaction, with the product distribution being influenced by the activating group on the enophile, the nature of the ene component, and the Lewis acid used. Activation of the enophile with an oxazolidinone function facilitated Lewis acid-catalysed cyclisation to afford mixtures of ene and hetero-Diels-Alder products. Activating the enophile with two ester groups gave a substrate that underwent a very facile ene cyclisation catalysed by MeAlCl2 to give the corresponding trans 3,4-disubstituted piperidines with diastereomeric ratios of > 200 : 1.

Details

Original languageEnglish
Pages (from-to)2925-2931
Number of pages7
JournalOrganic and Biomolecular Chemistry
Volume5
Issue number18
Publication statusPublished - 1 Jan 2007