University of Wollongong
Browse

Total synthesis of hyacinthacines B3, B4, and B 5 and purported hyacinthacine B7, 7-epi-hyacinthacine B7, and 7a-epi-hyacinthacine B3 from a common precursor

Download (416.09 kB)
journal contribution
posted on 2024-11-16, 06:57 authored by Kongdech Savaspun, Christopher Au, Stephen PyneStephen Pyne
The total synthesis of hyacinthacines B3, B4, and B5 and purported hyacinthacine B7, 7-epi-hyacinthacine B7, and 7a-epi-hyacinthacine B3 from a common anti-1,2-amino alcohol precursor is described. These syntheses confirmed that the proposed structures and absolute configurations of hyacinthacines B3, B4, and B5 were correct and disclosed that the proposed structure of hyacinthacine B7 was incorrect. Our synthetic and spectroscopic studies suggest that the natural hyacinthacines B5 and B7 are the same compounds; however, without access to authentic samples this cannot be unequivocally proven.

Funding

New strategies for the stereoselective synthesis of Stemona alkaloids and the discovery of new bioactive molecules

Australian Research Council

Find out more...

History

Citation

Savaspun, K., Au, C. W. G. & Pyne, S. G. (2014). Total synthesis of hyacinthacines B3, B4, and B 5 and purported hyacinthacine B7, 7-epi-hyacinthacine B7, and 7a-epi-hyacinthacine B3 from a common precursor. Journal of Organic Chemistry, 79 (10), 4569-4581.

Journal title

Journal of Organic Chemistry

Volume

79

Issue

10

Pagination

4569-4581

Language

English

RIS ID

90556

Usage metrics

    Categories

    Keywords

    Exports

    RefWorks
    BibTeX
    Ref. manager
    Endnote
    DataCite
    NLM
    DC