Synthesis of d-ribo-C-nucleoside analogues by dehydration of new d-allo-pentitol-1-yl heterocycles
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
Reference20 articles.
1. Acyclic-sugar pyrrole C-nucleoside-analogs derived from 2-(alkylamino)-2-deoxyaldoses
2. Preparation of C-nucleosides by dehydration of pentahydroxypentyl-heterocycles: Steric course and mechanism
3. New C-nucleoside analogs by dehydration of 1-benzyl-4,5,6,7-tetrahydro-6,6-dimethyl-2-(d-galacto-pentitol-1-yl)-indol-4-one
4. b R. Babiano Caballero and J.A. Galbis Perez, An. Quím. in press
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1. Lyxose and Ribose C -Glycosides;C-Furanosides;2018
2. Indium-mediated allylation in carbohydrate synthesis: A short and efficient approach towards higher 2-acetamido-2-deoxy sugars;Beilstein Journal of Organic Chemistry;2014-09-19
3. InCl3-catalyzed synthesis of C-pyrrolyl glycosides via tandem condensation of aminosugars and 1,3-dicarbonyl compounds in water;Tetrahedron Letters;2011-07
4. Acid-catalyzed dehydrative cyclization of 4-(d-galacto-pentitol-1-yl)-2-phenyl-2H-1,2,3-triazole. Synthesis and anomeric configuration of d-lyxo-C-nucleoside analogs;Carbohydrate Research;2001-01
5. The Chemistry of C-Nucleosides and Their Analogs I: C-Nucleosides of Hetero Monocyclic Bases;Advances in Heterocyclic Chemistry;1997
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