Unified Divergent Total Synthesis of Discorhabdin B, H, K, and Aleutianamine via the Late-Stage Oxidative N,S-Acetal Formation
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences, Tohoku University, Aoba 6-3, Aramaki, Aoba-ku, Sendai 980-8578, Japan
Funder
Japan Agency for Medical Research and Development
Japan Society for the Promotion of Science
Publisher
American Chemical Society (ACS)
Subject
Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis
Link
https://pubs.acs.org/doi/pdf/10.1021/jacs.3c06578
Reference64 articles.
1. Pyrroloiminoquinone and related metabolites from marine sponges
2. Discorhabdins and Pyrroloiminoquinone-Related Alkaloids
3. Chemistry, Chemotaxonomy and Biological Activity of the Latrunculid Sponges (Order Poecilosclerida, Family Latrunculiidae)
4. Cytotoxic pigments from new zealand sponges of the genus latrunculia : discorhabdins a, b and c
5. Discorhabdin D, an antitumor alkaloid from the sponges Latrunculia brevis and Prianos sp
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1. Divergent total syntheses of pyrroloiminoquinone alkaloids enabled by the development of a Larock/Buchwald–Hartwig annulation/cyclization;Chemical Science;2024
2. The Asymmetric Total Synthesis of Discorhabdin B, H, K, and Aleutianamine;Modern Natural Product Synthesis;2024
3. Total Synthesis of (+)‐Discorhabdin V**;Angewandte Chemie International Edition;2023-11-29
4. Total Synthesis of (+)‐Discorhabdin V**;Angewandte Chemie;2023-11-29
5. Total Synthesis of Aleutianamine;Journal of the American Chemical Society;2023-11-15
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