Diastereoselective enzymatic preparation of acetylated pentofuranosides carrying free 5-hydroxyl groups

Methyl 3-O-acetyl-2-deoxy-α-d-ribofuranoside, 1,3-di-O-acetyl-2-deoxy-α-d-ribofuranose and 1,2,3-tri-O-acetyl-α-d-arabinofuranose were diastereoselectively prepared (de = 100%) from anomeric mixtures of the corresponding 5-acetylated compounds through Candida antarctica B lipase (CAL B)-catalysed al...

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Detalles Bibliográficos
Publicado:	2009
Materias:	1,2,3 tri o acetyl alpha dextro arabinofuranose 1,3 di o acetyl 2 deoxy alpha dextro ribofuranose carbohydrate derivative hydroxyl group lipase B methyl 3 o acetyl 2 deoxy alpha dextro ribofuranoside unclassified drug acetylation alcoholysis article Candida antarctica diastereoisomer enzyme mechanism nonhuman priority journal quantum yield reaction analysis stereochemistry
Acceso en línea:	https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_09574166_v20_n15_p1813_Gudino http://hdl.handle.net/20.500.12110/paper_09574166_v20_n15_p1813_Gudino
Aporte de:	Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA) de Universidad de Buenos Aires

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