University of Wollongong
Browse

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

Download (683.14 kB)
journal contribution
posted on 2024-11-14, 15:44 authored by Thunwadee Ritthiwigrom, Anthony C Willis, Stephen PyneStephen Pyne
A flexible 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.

History

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. The Journal of Organic Chemistry, 75 (3), 815-824.

Journal title

Journal of Organic Chemistry

Volume

75

Issue

3

Pagination

815-824

Language

English

RIS ID

33602

Usage metrics

    Categories

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC