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
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Biochemistry,General Medicine,Analytical Chemistry
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1. Studies on saccharide benzimidazoles: 2-(β-D-gulofuranosyl)benzimidazole and 2-(β-D-glucofuranosyl)benzimidazole C-nucleoside analogs; synthesis, anomeric configuration and antifouling potency;Carbohydrate Research;2020-10
2. d - and l - altro - C -furanosides (II/ ent -II, α- C -Lyxose, α- C -Ribose);C-Furanosides;2018
3. Homo-C-nucleoside analogs IV. Synthesis of 4-(2,5-anhydro-D-altro-pentitol-1-yl)-2-phenyl-2H-1,2,3-triazole homo-C-nucleoside. CD assignment of the absolute configuration of the carbon bridge;Chirality;2017-01
4. Enantioseparation of nine indanone and tetralone derivatives by HPLC using carboxymethyl-β-cyclodextrin as the mobile phase additive;Chirality;2016-12-19
5. Synthesis of 2H-1,2,3-Triazoles;Topics in Heterocyclic Chemistry;2014
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