First synthesis of an ABCE ring substructure of daphnicyclidin A
Author:
Affiliation:
1. Department of Chemistry, University of Missouri-Columbia, Columbia, Missouri 65211, USA
Abstract
Funder
National Science Foundation
Publisher
Royal Society of Chemistry (RSC)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.rsc.org/en/content/articlepdf/2022/OB/D2OB01246D
Reference38 articles.
1. The Daphniphyllum alkaloids
2. Daphniphyllum Alkaloids: Recent Findings on Chemistry and Pharmacology
3. Recent Progress in the Chemistry of Daphniphyllum Alkaloids
4. Total Synthesis of Daphniphyllum Alkaloids: From Bicycles to Diversified Caged Structures
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1. Synthesis of the ABC Core of Daphniphyllum Alkaloids with a [5–6–7] Azatricyclic Scaffold via Ring Expansion of Azabicyclic and Azatricyclic Building Blocks;The Journal of Organic Chemistry;2024-07-01
2. Daphnicyclidin Alkaloids 2001–2023;European Journal of Organic Chemistry;2024-05-22
3. Total Synthesis of Four Classes of Daphniphyllum Alkaloids;Journal of the American Chemical Society;2023-11-30
4. Synthesis of the 5–6–7 Tricyclic Core of Daphnicyclidin-Type Alkaloids via a Tiffeneau–Demjanov Ring Enlargement Strategy;The Journal of Organic Chemistry;2023-10-06
5. Total Synthesis of (±)- and (−)-Daphnillonin B;Journal of the American Chemical Society;2023-05-11
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