Skip navigation
Skip navigation

Formal total synthesis of triptolide

Miller, Natalie; Willis, Anthony; Sherburn, Michael

Description

A new approach to the medicinally-important natural product triptolide is significantly shorter than previous syntheses, highly convergent and avoids the use of protecting groups; key features include two Diels-Alder reactions and a new deoxygenative aromatisation process.

CollectionsANU Research Publications
Date published: 2008
Type: Journal article
URI: http://hdl.handle.net/1885/50128
Source: Chemical Communications
DOI: 10.1039/b718754h

Download

File Description SizeFormat Image
01_Miller_Formal_total_synthesis_of_2008.pdf664.69 kBAdobe PDF    Request a copy


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

Updated:  12 November 2018/ Responsible Officer:  University Librarian/ Page Contact:  Library Systems & Web Coordinator