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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 OlivierWesley Olivier, Jason SmithJason Smith, Alexander BissemberAlexander BissemberThe 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 LettersVolume
24Issue
31Pagination
5772-5776ISSN
1523-7060Department/School
School of Natural SciencesPublisher
Amer Chemical SocPlace of publication
1155 16Th St, Nw, Washington, USA, Dc, 20036Rights statement
Copyright © 2022 American Chemical Society.Repository Status
- Restricted