Synthesis of 1-O-(Methylthio)thiocarbonyl Sugar Derivatives Bearing Acyl Protective Groups Using Phase Transfer Catalysis Methods
Author:
Affiliation:
1. a School of Dental Medicine, Tsurummi University , 2-1-3 Tsurumi, Tsurumi-ku, Yokohama, 230, Japan
2. b Department of Chemistry , Faculty of Science, Tokyo Institute of Technology , 2-12-1 Ookayama, Meguro-ku, Tokyo, 152, Japan
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/07328309708005757
Reference41 articles.
1. New and selective reactions and reagents in carbohydrate chemistry
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3. DEOXYGENATION OF SECONDARY ALCOHOLS: 3-DEOXY-1,2:5,6-DI-O-ISOPROPYLIDENE-a-d-ribo-HEXOFURANOSE
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1. Highly Reactive Glycosylation with 1-O-(Methylthio)thiocarbonyl Glycosyl Donors under Acidic to Neutral Reaction Conditions;The Journal of Organic Chemistry;2024-09-13
2. ChemInform Abstract: Synthesis of 1-O-(Methylthio)thiocarbonyl Sugar Derivatives Bearing Acyl Protective Groups Using Phase-Transfer Catalysis Methods.;ChemInform;2010-06-22
3. Degradation and Rearrangement Reactions;Glycoscience: Chemistry and Chemical Biology I–III;2001
4. Structure of anomeric glycosyl radicals and their transformations under reductive conditions;Advances in Carbohydrate Chemistry and Biochemistry;2000
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