An enantioselective double Diels - Alder approach to the tetracyclic framework of colombiasin A

Chaplin, Jason; Edwards, Alison; Flynn, Bernard

Cultural advice

The Australian National University acknowledges, celebrates and pays our respects to the Ngunnawal and Ngambri people of the Canberra region and to all First Nations Australians on whose traditional lands we meet and work, and whose cultures are among the oldest continuing cultures in human history.

Aboriginal and Torres Strait Islander peoples are advised that ANU Library collections may include images, names, voices, and other representations of deceased persons.

Material in the collection may contain terms, language or views that reflect the period in which the item was created and may be considered inappropriate today.

An enantioselective double Diels - Alder approach to the tetracyclic framework of colombiasin A

Date

2003

Authors

Chaplin, Jason

Edwards, Alison

Flynn, Bernard

Publisher

Royal Society of Chemistry

Abstract

The complex tetracyclic carbon skeleton of colombiasin A is conveniently accessed through an enantioselective intermolecular Diels-Alder-sulfoxide elimination-intra-molecular Diels-Alder (DA-E-IMDA) sequence.