Test environment running 7.6.6

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.

Towards the Total Synthesis of Vibsanin E, 15-O Methylcyclovibsanin B, 3-Hydroxyvibsanin E, Furanovibsanin A, and 3-O Methylfuranovibsanin A

Loading...
Thumbnail Image

Date

Authors

Schwartz, Brett
Tilly, David P
Heim, Ralf
Wiedemann, Stefan
Williams, Craig
Bernhardt, Paul

Journal Title

Journal ISSN

Volume Title

Publisher

Wiley-VCH Verlag GMBH

Abstract

Studies detailing synthetic approaches to a variety of biosynthetically related vibsanin-type diterpenes (i.e. vibsanin E, 15-O-methylcyclovibsanin B, 3-hydroxy-vibsanin E, furanovibsanin A, and 3-O-methylfuranovibsanin A) are discussed. Biogenetically modelled approaches are coupled with an investigation of classical and modern six- to seven-membered ring-expansion protocols, which gain access to the central core of these natural products.

Description

Citation

Source

European Journal of Organic Chemistry

Book Title

Entity type

Access Statement

License Rights

Restricted until

2037-12-31