Glycosylation studies on conformationally restricted 3,5-O-(di-tert- butylsilylene)-d-galactofuranosyl trichloroacetimidate donors for 1,2-cis α-d-galactofuranosylation

Conformationally restricted 3,5-O-di-tert-butylsilylene-d-galactofuranosyl trichloroacetimidate donors were synthesized from allyl α-d- galactofuranoside for the construction of 1,2-cis α-d-galactofuranosyl linkages. Glycosylation reactions were performed with several acceptors, including d-galacton...

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Detalles Bibliográficos
Publicado:	2011
Materias:	1,2-cis Galactofuranose Glycosylation Protecting groups Solvents effects Trichloroacetimidate Diethyl ethers Ethereal solvents Glycosylation reactions Reaction solvents Esterification Ethers Reaction intermediates Solvents 3,5 o (di tert butylsilylene) dextro galactofuranosyl trichloroacetimidate dextro galactono 1,4 lactone dichloromethane glucose derivative lactone derivative trichloroacetimidic acid unclassified drug article conformation glycosylation priority journal reaction analysis synthesis temperature Carbohydrate Conformation Furans Galactosides Organosilicon Compounds
Acceso en línea:	https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00086215_v346_n18_p2838_Tilve http://hdl.handle.net/20.500.12110/paper_00086215_v346_n18_p2838_Tilve
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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