Carbohydrates [electronic resource] : Synthesis, Mechanisms, and Stereoelectronic Effects /
Miljkovic, Momcilo.author.
Carbohydrates: Synthesis, Mechanisms, and Stereoelectronic Effects explains the conformational, electrostatic, and stereoelectronic factors that control the chemical and biochemical behavior of carbohydrates in living cells. Topics include the anomeric effect, the chemistry of the glycosidic bond, isomerization of free carbohydrates in aqueous solutions, relative reactivity of hydroxyl groups in carbohydrate molecules, and the addition of nucleophiles to glycopyranosiduloses. Focus then shifts to the synthesis of glycosidic bonds and oligosaccharides, the synthesis of anhydro and amino sugars, branched chain sugars and the protection of hydroxyl groups in monosaccharides. The last three chapters are devoted to areas often overlooked in carbohydrate chemistry textbooks: carbohydrate based antibiotics, synthesis of polychiral natural products from carbohydrates, and the chemistry of higher-carbon sugars.
Description based upon print version of record.
Includes bibliographical references and index.
Conformational Analysis of Monosaccharides -- Anomeric Effect -- Isomerization of Sugars -- Relative Reactivity of Hydroxyl Groups in Monosaccharides -- Cyclic Acetals and Ketals -- Nucleophilic Displacement and the Neighboring Group Participation -- Anhydrosugars -- Amino Sugars -- Oxidation of Monosaccharides -- Addition of Nucleophiles to Glycopyranosiduloses -- Chemistry of the Glycosidic Bond -- Synthesis of Polychiral Natural Products from Carbohydrates -- Carbohydrate-Based Antibiotics -- Higher-Carbon Monosaccharides.
Carbohydrates: Synthesis, Mechanisms, and Stereoelectronic Effects explains the conformational, electrostatic, and stereoelectronic factors that control the chemical and biochemical behavior of carbohydrates in living cells. Topics include the anomeric effect, the chemistry of the glycosidic bond, isomerization of free carbohydrates in aqueous solutions, relative reactivity of hydroxyl groups in carbohydrate molecules, and the addition of nucleophiles to glycopyranosiduloses. Focus then shifts to the synthesis of glycosidic bonds and oligosaccharides, the synthesis of anhydro and amino sugars, branched chain sugars and the protection of hydroxyl groups in monosaccharides. The last three chapters are devoted to areas often overlooked in carbohydrate chemistry textbooks: carbohydrate based antibiotics, synthesis of polychiral natural products from carbohydrates, and the chemistry of higher-carbon sugars.
Organic chemistry.
Polymers  .
Carbohydrates.
Bioorganic chemistry.
Organic Chemistry.
Polymer Sciences.
Carbohydrate Chemistry.
Bioorganic Chemistry.