Glycosyl iodides of protected d-glucosamine are generated in situ under mild conditions and coupled with different kinds of nucleophiles, providing the corresponding β-glycosides in good yields.

Efficient Synthesis of O-, S-, N- and C-Glycosides of 2-Amino-2-Deoxy-D-Glucopyranose from Glycosyl Iodides / N. Miquel, S. Vignando, G. Russo, L. Lay. - In: SYNLETT. - ISSN 0936-5214. - 2004:2(2004), pp. 341-343.

Efficient Synthesis of O-, S-, N- and C-Glycosides of 2-Amino-2-Deoxy-D-Glucopyranose from Glycosyl Iodides

S. Vignando;G. Russo
Penultimo
;
L. Lay
2004

Abstract

Glycosyl iodides of protected d-glucosamine are generated in situ under mild conditions and coupled with different kinds of nucleophiles, providing the corresponding β-glycosides in good yields.
Carbohydrates; Glycosyl iodides; Glycosylations; Stereoselective synthesis
Settore CHIM/06 - Chimica Organica
2004
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/145110
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