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Structural revision of parvistemoamide: informing biosynthetic proposals of Stemona alkaloids

journal contribution
posted on 2023-05-21, 11:40 authored by Wesley Olivier, Jason SmithJason Smith, Alexander BissemberAlexander Bissember
The natural product parvistemoamide was isolated in 1991 and has ostensibly eluded synthesis. Its distinctive assigned structure represents the first and only Stemona alkaloid within its class. For over 30 years, this structure has influenced biosynthetic proposals concerning this family of natural products. Following synthetic studies and comprehensive analysis of relevant literature, a revised structure of parvistemoamide is proposed that is consistent with the fundamental Stemona alkaloid stemoamide.

Funding

Australian Research Council

History

Publication title

Organic Letters

Volume

24

Issue

31

Pagination

5772-5776

ISSN

1523-7060

Department/School

School of Natural Sciences

Publisher

Amer Chemical Soc

Place of publication

1155 16Th St, Nw, Washington, USA, Dc, 20036

Rights statement

Copyright © 2022 American Chemical Society.

Repository Status

  • Restricted

Socio-economic Objectives

Expanding knowledge in the chemical sciences

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