Sugar chemistry without protecting groups: A regioselective addition of the primary hydroxyl of monosaccharides to alkylisocyanates
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference13 articles.
1. Relative Reactivities of Hydroxyl Groups in Carbohydrates
2. Facile enzymatic preparation of monoacylated sugars in pyridine
3. Chimie des sucres sans groupements protecteurs - I - esterification regioselective de l'hydroxyle anomere du lactose, du maltose et du glucose
4. Synthesis of D-glucosyl esters, using unprotected β-D-glucose
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2. Carbohydrate-Based Amphiphiles: Resource for Bio-based Surfactants;Green Chemistry and Chemical Engineering;2019
3. 2-O-N-Benzylcarbamoyl as a Protecting Group To Promote β-Selective Glycosylation and Its Applications in the Stereoselective Synthesis of Oligosaccharides;The Journal of Organic Chemistry;2018-03-07
4. Carbohydrate-Based Amphiphiles: Resource for Bio-based Surfactants;Encyclopedia of Sustainability Science and Technology;2018
5. Protecting-Group-Free One-Pot Synthesis of Glycoconjugates Directly from Reducing Sugars;Angewandte Chemie International Edition;2014-09-08
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