Total synthesis of the proposed structure of decurrenside D
Author:
Funder
CONACYT
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Benzyl Benzoate Glycoside and 3-Deoxy-d-manno-2-octulosonic Acid Derivatives from Solidago decurrens
2. Constrained 3,6-Anhydro-Heptosides: Synthesis by a DAST-Induced Debenzylative Reaction, and Reactivity Profile
3. Total Synthesis of Cephalosporolide E via a Tandem Radical/Polar Crossover Reaction. The Use of the Radical Cations under Nonoxidative Conditions in Total Synthesis
4. High 1,3-trans Stereoselectivity in Nucleophilic Substitution at the Anomeric Position and β-Fragmentation of the Primary Alkoxyl Radical in 3-Amino-3-deoxy-ribofuranose Derivatives: Application to the Synthesis of 2-epi-(−)-Jaspine B
5. A five-step formal synthesis of (−)-Jaspine B
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1. Nucleophilic substitution at the anomeric position of furanose carbohydrates. The case of the C-allylations;Carbohydrate Research;2021-12
2. Recent trends in the structural revision of natural products;Natural Product Reports;2018
3. Computer-Guided Total Synthesis of Natural Products. Recent Examples and Future Perspectives;Journal of the Brazilian Chemical Society;2018
4. Structure Revision of Decurrensides A–E Enabled by the RFF Parametric Calculations of Proton Spin–Spin Coupling Constants;The Journal of Organic Chemistry;2016-09-08
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