Reaction of Some 1-Deoxy-2,3-Dicarbonyl Hexose Derivatives with Aminoguanidine (Guanylhydrazine)1
Author:
Publisher
Informa UK Limited
Subject
Organic Chemistry,Biochemistry
Link
http://www.tandfonline.com/doi/pdf/10.1080/10256018808623883
Reference18 articles.
1. Formation of 1-deoxy-d-erythro-2,3-hexodiulose from Amadori compounds
2. Formation of 1-amino-1,4-dideoxy-2,3-hexodiuloses and 2-aminoacetylfurans in the Maillard reaction
3. Synthesis of a Derivative of 1-Deoxy-2,3-D-Threo-(and D-Erythro) Hexodiulose, an Intermediate in the Acid and Base Catalyzed Degradation of Hexoses
4. Aminoguanidine Prevents Diabetes-Induced Arterial Wall Protein Cross-Linking
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1. Cycloamination strategies for renewable N-heterocycles;Green Chemistry;2020
2. ChemInform Abstract: Reaction of Some 1-Deoxy-2,3-dicarbonyl Hexose Derivatives with Aminoguanidine (Guanylhydrazine).;ChemInform;2010-08-12
3. Manipulation of Carbohydrate Carbon Atoms for the Synthesis of Heterocycles;Heterocycles from Carbohydrate Precursors;2007
4. Correlations between Structure and Reactivity of Amadori Compounds: the Reactivity of Acyclic Forms;The Maillard Reaction in Foods and Medicine;2005
5. Detection of α-Dicarbonyl Compounds in Maillard Reaction Systems and in Vivo;Journal of Agricultural and Food Chemistry;2001-10-31
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