Total Synthesis of Spiroketal Alkaloids Lycibarbarines A–C
Author:
Affiliation:
1. School of Chemical Sciences, University of Auckland, 23 Symonds Street, Auckland 1010, New Zealand
2. Maurice Wilkins Centre for Molecular Biodiscovery, 3 Symonds Street, Auckland 1010, New Zealand
Funder
University of Auckland
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.3c00902
Reference32 articles.
1. Lycibarbarines A–C, Three Tetrahydroquinoline Alkaloids Possessing a Spiro-Heterocycle Moiety from the Fruits of Lycium barbarum
2. Synthetic approaches to access acortatarins, shensongines and pollenopyrroside; potent antioxidative spiro-alkaloids with a naturally rare morpholine moiety
3. N-Alkynyl Pyrrole Based Total Synthesis of Shensongine A
4. 2-Formylpyrrole natural products: origin, structural diversity, bioactivity and synthesis
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1. Brønsted acid catalyzed [4 + 2] cycloaddition for the synthesis of bisbenzannulated spiroketals with antifungal activities;Organic & Biomolecular Chemistry;2024
2. Total Synthesis of Spiroalkaloids Lycibarbarines A–C;European Journal of Organic Chemistry;2023-07-28
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