Synthesis of some O-, S- and N-glycosides of hept-2-ulopyranosonamides |
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| Authors: | Veronika Nagy,Katalin Czifrá k,Lá szló Somsá k |
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| Affiliation: | a Department of Organic Chemistry (POB 20), University of Debrecen, H-4010 Debrecen, Hungary
b Department of Physical Chemistry (POB 7), University of Debrecen, H-4010 Debrecen, Hungary |
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| Abstract: | (O-Peracylated α-d-gluco- and -galacto-hept-2-ulopyranosylbromide)onamides gave the corresponding (alkyl β-d-glyco-hept-2-ulopyranoside)onamides under Koenigs-Knorr conditions, and similar aryl glycosides were obtained with sodium phenolates; (aryl and hetaryl 2-thio-β-d-gluco-hept-2-ulopyranoside)onamides were formed with thiophenols in the presence of K2CO3 in acetone, and reactions with aniline in CH2Cl2 furnished (N-phenyl β-d-glyco-hept-2-ulopyranosylamine)onamides. Some deprotected derivatives of d-gluco configuration obtained by the Zemplén protocol showed no significant inhibition against rabbit muscle glycogen phosphorylase b. |
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| Keywords: | Hept-2-ulopyranosonamides O-glycoside S-glycoside N-glycoside |
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