Skip navigation
Skip navigation

Application of an Intramolecular Stetter Reaction to Access trans,syn,trans -Fused Pyrans

McErlean, Christopher S P; Willis, Anthony


The use of a commercially available thiazolium salt facilitated an intramolecular Stetter reaction between an aliphatic aldehyde and an acrylate unit, which delivered a trans,syn-fused bicyclic pyranone in high yield as a single diastereomer. The pyranone was used to synthesize a trans,syn,trans-fused polycyclic ether array and was ring expanded to give the corresponding oxepanone.

CollectionsANU Research Publications
Date published: 2009
Type: Journal article
Source: Synlett
DOI: 10.1055/s-0028-1087519


File Description SizeFormat Image
01_McErlean_Application_of_an_2009.pdf101.93 kBAdobe PDFThumbnail

Items in Open Research are protected by copyright, with all rights reserved, unless otherwise indicated.

Updated:  17 November 2022/ Responsible Officer:  University Librarian/ Page Contact:  Library Systems & Web Coordinator