The profound effect of substituents at C-5 of glycosyl sialosides on their stereoselectivity is well-known although the exact nature of this effect is somewhat less understood. Presented herein is a comparative study of a range of novel sialyl donors with various O-substituents. It is demonstrated that O-substituents at C-4 and C-7 may also have a significant effect on the reactivity of sialyl donors and on the stereoselectivity of chemical sialylation
The stereoselective synthesis of beta-mannosides and the underlying reaction mechanism have been tho...
The stereoselective synthesis of beta-mannosides and the underlying reaction mechanism have been tho...
Novel oxathiane spiroketal donors have been synthesised and activated via an umpolung S-arylation st...
Sialic acids are a family of forty-three carbohydrates frequently expressed at the terminal position...
Two <i>N</i>-acetyl 4<i>O</i>,5<i>N</i>-oxazolidinone-protected sialyl thioglycosides epimeric at th...
The tuning effect of silyl protecting groups on the glycosylation reactivity of arabinofuranosyl phe...
Two phosphite sialyl donors, each having an auxiliary 3-(S)-phenylseleno group, were prepared and ev...
Sialic acid is a family of carbohydrates derived from neuraminic acid. This sugar is unique in many ...
With the picolinyl (Pic) group as a C-1 located directing group and N3 as versatile precursor for C5...
<i>N</i>-Acetyl 4-<i>O</i>,5-<i>N</i>-oxazolidinone protected sialyl phosphates of either anomeric c...
A new sialyl donor, N,N-dibenzyl-protected p-toluenethiosialoside, was synthesized and its sialylati...
The outcome of a glycosylation reaction critically depends on the reactivity of all reaction partner...
A new sialyl donor, N,N-acetyl, benzoyl-O-perbenzoyl-protected p-toluenethiosialoside, was synthesiz...
The stereoselective synthesis of beta-mannosides and the underlying reaction mechanism have been tho...
The stereoselective synthesis of beta-mannosides and the underlying reaction mechanism have been tho...
The stereoselective synthesis of beta-mannosides and the underlying reaction mechanism have been tho...
The stereoselective synthesis of beta-mannosides and the underlying reaction mechanism have been tho...
Novel oxathiane spiroketal donors have been synthesised and activated via an umpolung S-arylation st...
Sialic acids are a family of forty-three carbohydrates frequently expressed at the terminal position...
Two <i>N</i>-acetyl 4<i>O</i>,5<i>N</i>-oxazolidinone-protected sialyl thioglycosides epimeric at th...
The tuning effect of silyl protecting groups on the glycosylation reactivity of arabinofuranosyl phe...
Two phosphite sialyl donors, each having an auxiliary 3-(S)-phenylseleno group, were prepared and ev...
Sialic acid is a family of carbohydrates derived from neuraminic acid. This sugar is unique in many ...
With the picolinyl (Pic) group as a C-1 located directing group and N3 as versatile precursor for C5...
<i>N</i>-Acetyl 4-<i>O</i>,5-<i>N</i>-oxazolidinone protected sialyl phosphates of either anomeric c...
A new sialyl donor, N,N-dibenzyl-protected p-toluenethiosialoside, was synthesized and its sialylati...
The outcome of a glycosylation reaction critically depends on the reactivity of all reaction partner...
A new sialyl donor, N,N-acetyl, benzoyl-O-perbenzoyl-protected p-toluenethiosialoside, was synthesiz...
The stereoselective synthesis of beta-mannosides and the underlying reaction mechanism have been tho...
The stereoselective synthesis of beta-mannosides and the underlying reaction mechanism have been tho...
The stereoselective synthesis of beta-mannosides and the underlying reaction mechanism have been tho...
The stereoselective synthesis of beta-mannosides and the underlying reaction mechanism have been tho...
Novel oxathiane spiroketal donors have been synthesised and activated via an umpolung S-arylation st...