A simple, efficient, stereoselective synthesis of deoxyaminothreopentopyranoside I, corresponding to the monosaccharide unit (E ring) of calicheamicin, from Me 2-deoxy-β-D-ribopyranoside in 6 steps in yield 60%, is described.
An efficient stereoselective synthesis of the amino sugar component (E ring) of calicheamicin gamma(I)(1)
CROTTI, PAOLO;DI BUSSOLO, VALERIA;FAVERO, LUCILLA;PINESCHI, MAURO
1996-01-01
Abstract
A simple, efficient, stereoselective synthesis of deoxyaminothreopentopyranoside I, corresponding to the monosaccharide unit (E ring) of calicheamicin, from Me 2-deoxy-β-D-ribopyranoside in 6 steps in yield 60%, is described.File in questo prodotto:
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