Differentiation of specific positions in axial-symmetrical cyclodextrins (CDs), exhibiting a dense display of identical functional groups, is challenging. A novel strategy toward this goal that exploits a solid matrix to display the complementary reagent functionalities sufficiently far from each other to prevent CDs from reacting through more than one site is reported. Using a “catch-and-release” process based on the Staudinger reaction, the utility of this concept to easily produce complex CD functionalization patterns in one pot and without any purification step is demonstrated
International audienceAccess to C-n (n > 4) symmetric cyclic concave molecules with a different func...
A simple and efficient radical C–H functionalization to access modified cyclodextrins (CDs) has been...
β-Cyclodextrin (β-CD) dimers have been prepared using the bioorthogonal Staudinger ligation for the ...
International audienceFour different regioselective double capping reactions were applied either to ...
A first solid phase approach to obtain monosubstituted CD conjugates to different labels has been de...
A first solid phase approach to obtain monosubstituted CD conjugates to different labels has been de...
International audienceMethylated - and -cyclodextrin skeletons were both equipped with an unsymmetri...
A simple and efficient radical C–H functionalization to access modified cyclodextrins (CDs) has been...
This crit. review is a report of recent applications concerning the CD derivs. and their metal compl...
Cyclodextrins (CDs) are naturally occurring macrocyclic oligosaccharides comprised of α-1,4 linked g...
This master thesis deals with preparation of cyclodextrin (CD) derivatives that are suitable for bon...
International audienceDynamic systems of cyclodextrins (CDs) enabled by a native cyclodextrin glucan...
The use of cyclodextrins (CDs) in the textile field has been growing since the 1980s. Derivatives, ...
221 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2006.Cyclodextrins (CDs) are amphi...
The synthesis of batch-to-batch reproducible cyclodextrin (CD) derivatives often requires functional...
International audienceAccess to C-n (n > 4) symmetric cyclic concave molecules with a different func...
A simple and efficient radical C–H functionalization to access modified cyclodextrins (CDs) has been...
β-Cyclodextrin (β-CD) dimers have been prepared using the bioorthogonal Staudinger ligation for the ...
International audienceFour different regioselective double capping reactions were applied either to ...
A first solid phase approach to obtain monosubstituted CD conjugates to different labels has been de...
A first solid phase approach to obtain monosubstituted CD conjugates to different labels has been de...
International audienceMethylated - and -cyclodextrin skeletons were both equipped with an unsymmetri...
A simple and efficient radical C–H functionalization to access modified cyclodextrins (CDs) has been...
This crit. review is a report of recent applications concerning the CD derivs. and their metal compl...
Cyclodextrins (CDs) are naturally occurring macrocyclic oligosaccharides comprised of α-1,4 linked g...
This master thesis deals with preparation of cyclodextrin (CD) derivatives that are suitable for bon...
International audienceDynamic systems of cyclodextrins (CDs) enabled by a native cyclodextrin glucan...
The use of cyclodextrins (CDs) in the textile field has been growing since the 1980s. Derivatives, ...
221 p.Thesis (Ph.D.)--University of Illinois at Urbana-Champaign, 2006.Cyclodextrins (CDs) are amphi...
The synthesis of batch-to-batch reproducible cyclodextrin (CD) derivatives often requires functional...
International audienceAccess to C-n (n > 4) symmetric cyclic concave molecules with a different func...
A simple and efficient radical C–H functionalization to access modified cyclodextrins (CDs) has been...
β-Cyclodextrin (β-CD) dimers have been prepared using the bioorthogonal Staudinger ligation for the ...