Aldol type reaction of unprotected sugars in methanol
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference6 articles.
1. Selective Monoesterification of Unprotected Mono and Disaccharides
2. Carbon-carbon bond formation in aqueous ethanol: diastereoselective transformation of unprotected carbohydrates to higher carbon sugars using allyl bromide and tin metal
3. Chemie von a-Aminonitrilen. Aldomerisierung von Glycolaldehyd-phosphat zu racemischen Hexose-2,4,6-triphosphaten und (in Gegenwart von Formaldehyd) racemischen Pentose-2,4-diphosphaten: rac-Allose-2,4,6-triphosphat und rac-Ribose-2,4-diphosphat sind die R
4. Synthesis of threo- and erythro-3-pentulose by aldol type reaction in water
5. Stereoselectivity in the Triose Aldol Condensation and the Aldol Condensation Between Glyceraldehyde and Glycolaldehyde
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3. Tin-catalyzed conversion of biomass-derived triose sugar and formaldehyde to α-hydroxy-γ-butyrolactone;Chemical Communications;2014
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5. Total Syntheses of Carbohydrates: Organocatalyzed Aldol Additions of Dihydroxyacetone;Chemistry - A European Journal;2007-10-31
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