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.

Total synthesis of uniflorine A, casuarine, australine, 3-epi-australine, and 3,7-di-epi-australine from a common precursor

Thumbnail Image

Date

2010-02-05

Authors

Pyne, Stephen G.

Journal Title

Journal ISSN

Volume Title

Publisher

Abstract

(Chemical Equation Presented) Aflexible method for the diastereoselective total synthesis of the pyrrolizidine alkaloids uniflorine A, casuarine, australine, and 3-epi-australine and the unnatural epimer 3,7-di-epi-australine from a common chiral 2,5-dihydropyrrole precursor is described.

Description

Keywords

Organic Chemistry

Citation

Ritthiwigrom , T , Willis , A C & Pyne , S G 2010 , ' Total synthesis of uniflorine A, casuarine, australine, 3-epi-australine, and 3,7-di-epi-australine from a common precursor ' , Journal of Organic Chemistry , vol. 75 , no. 3 , pp. 815-824 . https://doi.org/10.1021/jo902355p

URI

https://dspace-test.anu.edu.au/handle/1885/733712353

Collections

Pure Test Collection

Source

Type

/dk/atira/pure/researchoutput/researchoutputtypes/contributiontojournal/article

Book Title

Journal of Organic Chemistry

Entity type

Access Statement

License Rights

DOI

Restricted until

DSpace software copyright © 2002-2026 LYRASIS