N-Glycosidation of d-arabino-hex-2-ulosonic acid
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference7 articles.
1. Reductive cyclization of carbohydrate 2-nitrophenylhydrazones to chiral functionalized 1,2,4-benzotriazines and benzimidazoles
2. Methyl d-arabino-hex-2-ulopyranosonate as a building block for spiro[1,4-benzoxazine-2,2′-pyrans]
3. Synthesis of spiro[1,4-benzothiazine-2,2′-pyrans] starting from methyl β-D-arabino-2-hexulopyranosonate
4. Synthesis of spiro[pyrido[3,2-b][1,4]oxazin-2,2′-pyrans] based upon methyld-arabino-2-hexulopyranosonate
5. Optimierte Synthesen f�r Methyl- und Natrium-2-oxo-D-gluconat als Synthesebausteine
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1. Microbiologically Produced Carboxylic Acids Used as Building Blocks in Organic Synthesis;Subcellular Biochemistry;2012
2. A convenient synthesis of hexulosonic acids by IBX mediated oxidation of D-glucono-1,5-lactone derivatives;Arkivoc;2011-03-13
3. Stereocontrolled synthesis of thiohydantoin spironucleosides from sugar spiroacetals;Tetrahedron;2006-01
4. Heterocycles from Carbohydrate Isothiocyanates;Heterocycles from Carbohydrate Precursors;2006
5. Synthesis and Transformation of Glycosyl Azides;Advances in Carbohydrate Chemistry and Biochemistry Volume 60;2006
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