Cyclopropanation of glycals: Application to the synthesis of 2-deoxy-2-vinyl glycosides
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference15 articles.
1. 4,6-O-Benzylidene-3-deoxy-3-C-(iodomethyl)-D-allal: precursor of a cyclopropylcarbinyl-oxo-carbonium ion
2. Cyclopropylcarbinyl-oxo-carboniumions. A solvolytic basis for the cyclopropylcarbinyl-oxo-carbonium ion
3. The Synthesis of some α-Cyclopropylcarbonyl Glycopyranosides
4. Cyclopropylcarbinyl-oxo-carbonium Ions. Part V. Synthesis and Chemistry of some Cyclopropyl Glycopyranosides
5. Cyclopropylcarbinyl-oxo-carbonium Ions. Part VI. Synthesis and Chemistry of an Epimeric Pair of Homoallyl Iodides (3-Iodomethyl Glycals)
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1. Simple Synthesis of 1,2‐Dideoxy‐2‐Vinyl Carbohydrates by Tin‐Free Radical Reactions of Xanthates;Chemistry – A European Journal;2023-11-10
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3. Radical Clock Probes to Determine Carbohydrate Radical Stabilities;Organic Letters;2020-02-03
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5. Reactions of 1,2-cyclopropyl carbohydrates;Pure and Applied Chemistry;2014-09-19
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