Alkyl thio-, phenyl seleno-, and phenyl thioglycosides can be prepared through short synthetic sequences based on the generation of glycosyl iodides as versatile intermediates. In addition, a novel cheap combined system (stoichiometric NBS and catalytic Bi(OTf)(3)) has been developed for rapid and efficient activation of a wide variety of thio- and selenoglycoside donors.

Novel approaches for the synthesis and activation of thio- and selenoglycoside donors / Valerio, Silvia; Iadonisi, Alfonso; Adinolfi, Matteo; Ravida', Alessandra. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 72:(2007), pp. 6097-6106.

Novel approaches for the synthesis and activation of thio- and selenoglycoside donors

VALERIO, SILVIA;IADONISI, ALFONSO;ADINOLFI, MATTEO;RAVIDA', ALESSANDRA
2007

Abstract

Alkyl thio-, phenyl seleno-, and phenyl thioglycosides can be prepared through short synthetic sequences based on the generation of glycosyl iodides as versatile intermediates. In addition, a novel cheap combined system (stoichiometric NBS and catalytic Bi(OTf)(3)) has been developed for rapid and efficient activation of a wide variety of thio- and selenoglycoside donors.
2007
Novel approaches for the synthesis and activation of thio- and selenoglycoside donors / Valerio, Silvia; Iadonisi, Alfonso; Adinolfi, Matteo; Ravida', Alessandra. - In: JOURNAL OF ORGANIC CHEMISTRY. - ISSN 0022-3263. - STAMPA. - 72:(2007), pp. 6097-6106.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/204445
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