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1	A latent-active glycosylation approach for the synthesis of saccharides derived from the capsular polysaccharide of group B Streptococcus type IA Bai, Yu January 2000 (has links) No description available. 547
2	Boronate esters in oligosaccharide synthesis Belogi, Gianluca January 2000 (has links) No description available. 547
3	Protecting Group-free Synthesis of Glycosides Paul, Caroline Emilie 20 March 2012 (has links) Carbohydrates play major roles in many biological processes. Therefore, the synthesis of oligosaccharides is of considerable interest for biological, medicinal, and pharmacological studies. Many approaches have been developed for the synthesis of oligosaccharides, in which the main focus is often the formation of the glycosidic bonds. Traditional approaches use protecting group strategies that can be time consuming and can result in poor overall yield. This thesis describes the protecting group-free synthesis of a series of glycosyl donors of a range of mono- and disaccharides. These donors can be used to synthesize unprotected glycosyl chlorides, observed in situ. Reaction of the glycosyl chlorides with a variety of nucleophiles afforded the expected displacement products, giving access to a range of O-, N-, and S-linked glycosides, without resorting to the use of protecting groups. Protecting group-free glycosidations Unprotected glycosyl chlorides Glycosyl donors 0490
4	Protecting Group-free Synthesis of Glycosides Paul, Caroline Emilie 20 March 2012 (has links) Carbohydrates play major roles in many biological processes. Therefore, the synthesis of oligosaccharides is of considerable interest for biological, medicinal, and pharmacological studies. Many approaches have been developed for the synthesis of oligosaccharides, in which the main focus is often the formation of the glycosidic bonds. Traditional approaches use protecting group strategies that can be time consuming and can result in poor overall yield. This thesis describes the protecting group-free synthesis of a series of glycosyl donors of a range of mono- and disaccharides. These donors can be used to synthesize unprotected glycosyl chlorides, observed in situ. Reaction of the glycosyl chlorides with a variety of nucleophiles afforded the expected displacement products, giving access to a range of O-, N-, and S-linked glycosides, without resorting to the use of protecting groups. Protecting group-free glycosidations Unprotected glycosyl chlorides Glycosyl donors 0490
5	Synthesis of conjugates of L-fucose and ortho-carborane as potential agents for boron neutron capture therapy and synthesis of 2,3-dideoxy-2,3-methanoribofuranoside glycosyl donors and a study of their use in stereocontrolled glycosylation reactions Basak, Prakriti 10 February 2003 (has links) No description available. Chemistry, Organic boron neutron capture therapy stereocontrolled glycosylation reactions

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