A mild and effective method for the synthesis of polyhydroxylated quinolizidine iminosugars is described. The Mannich-type reaction of iminosugar C-glycosides with aldehyde in the presence of L-proline-Et3N provides polyhydroxylated quinolizidine iminosugars, and desired products as the potential glucosidase inhibitors were obtained in good to excellent yields with excellent stereoselectivity
International audienceA highly enantioselective synthesis of (R,S) or (S,S)-2,6-disubstituted dehydr...
Design and preparation of novel bioactive compounds for development of new drug leads is a challengi...
This manuscript describes the synthesis and bioevaluation of 10 new iminosugars. Iminosugars are an ...
A series of new N-substituted iminosugars were successfully synthesized through a general synthetic ...
An effective and facile method for the synthesis of N-substituted trihydroxypiperidine derivatives i...
A direct approach to the synthesis of indolizidine and quinolizidine scaffolds of iminosugars is des...
A direct approach to the synthesis of indolizidine and quinolizidine scaffolds of iminosugars is des...
The concise enantioselective syntheses of iminolyxitol and iminoribitol glycosidase inhibitors start...
The individual sugars that constitute more complex carbo-hydrates are joined together by glycosidic ...
The individual sugars that constitute more complex carbo-hydrates are joined together by glycosidic ...
The individual sugars that constitute more complex carbo-hydrates are joined together by glycosidic ...
International audienceA highly enantioselective synthesis of (R,S) or (S,S)-2,6-disubstituted dehydr...
International audienceA highly enantioselective synthesis of (R,S) or (S,S)-2,6-disubstituted dehydr...
Design and preparation of novel bioactive compounds for development of new drug leads is a challengi...
International audienceA highly enantioselective synthesis of (R,S) or (S,S)-2,6-disubstituted dehydr...
International audienceA highly enantioselective synthesis of (R,S) or (S,S)-2,6-disubstituted dehydr...
Design and preparation of novel bioactive compounds for development of new drug leads is a challengi...
This manuscript describes the synthesis and bioevaluation of 10 new iminosugars. Iminosugars are an ...
A series of new N-substituted iminosugars were successfully synthesized through a general synthetic ...
An effective and facile method for the synthesis of N-substituted trihydroxypiperidine derivatives i...
A direct approach to the synthesis of indolizidine and quinolizidine scaffolds of iminosugars is des...
A direct approach to the synthesis of indolizidine and quinolizidine scaffolds of iminosugars is des...
The concise enantioselective syntheses of iminolyxitol and iminoribitol glycosidase inhibitors start...
The individual sugars that constitute more complex carbo-hydrates are joined together by glycosidic ...
The individual sugars that constitute more complex carbo-hydrates are joined together by glycosidic ...
The individual sugars that constitute more complex carbo-hydrates are joined together by glycosidic ...
International audienceA highly enantioselective synthesis of (R,S) or (S,S)-2,6-disubstituted dehydr...
International audienceA highly enantioselective synthesis of (R,S) or (S,S)-2,6-disubstituted dehydr...
Design and preparation of novel bioactive compounds for development of new drug leads is a challengi...
International audienceA highly enantioselective synthesis of (R,S) or (S,S)-2,6-disubstituted dehydr...
International audienceA highly enantioselective synthesis of (R,S) or (S,S)-2,6-disubstituted dehydr...
Design and preparation of novel bioactive compounds for development of new drug leads is a challengi...
This manuscript describes the synthesis and bioevaluation of 10 new iminosugars. Iminosugars are an ...