Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/16962
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Título : Fragmentation of carbohydrate anomeric alkoxy radicals. Tandem β-fragmentation-cyclization of alcohols
Autor : Armas, Pedro de, Francisco, Cosme G., Suárez, Ernesto
Fecha de publicación : Sep-1993
Editor: American Chemical Society
Resumen: In recent years there has been a growing interest in carbohydrates as synthetic precursors to enantiomerically pure bioactive molecules because of their well-defined stereochemistry, highly functionalized nature, and distinct reactivities of the hydroxyl groups. We consider worthwhile a general procedure to obtain cyclic carbohydrates, even those not easily accessible by other routes, with a masked hydroxy aldehyde, the elaboration of which may be conveniently timed and whose functionalities would each be eligible for further elaboration.
Descripción : 2 pages, 1 table, 1 scheme.
Versión del editor: http://dx.doi.org/10.1021/ja00072a060
URI : http://hdl.handle.net/10261/16962
ISSN: 0002-7863
DOI: 10.1021/ja00072a060
Citación : Journal of the American Chemical Society 115(19): 8865-8866 (1993)
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