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Please use this identifier to cite or link to this item: http://hdl.handle.net/10261/17602
Title: Fragmentation of carbohydrate anomeric alkoxy radicals. Synthesis of azasugars
Authors: Francisco, Cosme G. ; Freire, Raimundo ; González Martín, Concepción C. ; Suárez, Ernesto
Issue Date: 27-Jun-1997
Publisher: Elsevier
Citation: Tetrahedron Asymmetry 8(12): 1971-1974 (1997)
Abstract: The reaction of conveniently protected 5-amino-5-deoxy pentoses and 6-amino-6-deoxy hexoses with iodosylbenzene and iodine is an efficient method, via β-fragmentation of the anomeric alkoxy radicals, for the synthesis of azasugars of the tetrose and pentose series, respectively.
Description: 4 pages, 1 table, 1 scheme.
Publisher version (URL): http://dx.doi.org/10.1016/S0957-4166(97)00188-2
URI: http://hdl.handle.net/10261/17602
ISSN: 0957-4166
DOI: 10.1016/S0957-4166(97)00188-2
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