Effective activation of 'armed' thioglycoside with a new combination of trityl tetrakis(pentafluorophenyl)borate [TrB(C6F5)(4)] and N-(ethylthio)phthalimide (PhthNSEt)
H. Jona et al., Effective activation of 'armed' thioglycoside with a new combination of trityl tetrakis(pentafluorophenyl)borate [TrB(C6F5)(4)] and N-(ethylthio)phthalimide (PhthNSEt), CHEM LETT, (10), 2000, pp. 1178-1179
Glycosylation of the 'armed' thioglycoside with various glycosyl accepters
is promoted by using a combination of stoichiometoric amount of N-(ethylthi
o)phthalimide (PhthNSEt) and catalytic amount of trityl tetrakis(pentafluor
ophenyl)borate [TrB(C6F5)(4)], and is successfully applied to one-pot 'arme
d-disarmed' sequential synthesis of trisaccharides.