Fragmentation of carbohydrate anomeric alkoxy radicals. A new general synthesis of cyclic ketoses
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference20 articles.
1. Formation of convenient chiral intermediates from carbohydrates and their use in synthesis
2. Synthesis of medium-sized lactones: Iodosobenzene diacetate an efficient reagent for β-fragmentation of alkoxy-radicals
3. Hypervalent organoiodine compounds: radical fragmentation of oxabicyclic hemiacetals. Convenient synthesis of medium-sized and spiro lactones
4. Reagents with Hypervalent Iodine: Formation of Convenient Chiral Synthetic Intermediates by Fragmentation of Carbohydrate Anomeric Alkoxy Radicals
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1. Formation of Ethers by Acetal, Carbonyl, and Ortho Ester Conversions;Comprehensive Organic Transformations;2018-02-28
2. Synthesis of Branched Iminosugars through a Hypervalent Iodine(III)-Mediated Radical-Polar Crossover Reaction;The Journal of Organic Chemistry;2013-07-25
3. Concise Entry to Chiral 5-(4-Hydroxybutyl)-2(5H)-furanone via HTIB-Mediated Novel Oxidative Fragmentation: Formal Total Synthesis of (+)-Dubiusamine A;Organic Letters;2013-03-26
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5. ChemInform Abstract: Fragmentation of Carbohydrate Anomeric Alkoxy Radicals. A New General Synthesis of Cyclic Ketoses.;ChemInform;2010-08-19
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