Year |
Citation |
Score |
2017 |
Henkel S, Misuraca MC, Ding Y, Guitet M, Hunter CA. Enhanced Chelate Cooperativity in Polar Solvents. Journal of the American Chemical Society. PMID 28467069 DOI: 10.1021/Jacs.7B01765 |
0.722 |
|
2017 |
Zhang P, Tugny C, Meijide Suárez J, Guitet M, Derat E, Vanthuyne N, Zhang Y, Bistri O, Mouriès-Mansuy V, Ménand M, Roland S, Fensterbank L, Sollogoub M. Artificial Chiral Metallo-pockets Including a Single Metal Serving as Structural Probe and Catalytic Center Chem. 3: 174-191. DOI: 10.1016/J.Chempr.2017.05.009 |
0.681 |
|
2014 |
Wang B, Zaborova E, Guieu S, Petrillo M, Guitet M, Blériot Y, Ménand M, Zhang Y, Sollogoub M. Site-selective hexa-hetero-functionalization of α-cyclodextrin an archetypical C₆-symmetric concave cycle. Nature Communications. 5: 5354. PMID 25382259 DOI: 10.1038/Ncomms6354 |
0.645 |
|
2013 |
Guitet M, Zhang P, Marcelo F, Tugny C, Jiménez-Barbero J, Buriez O, Amatore C, Mouriès-Mansuy V, Goddard JP, Fensterbank L, Zhang Y, Roland S, Ménand M, Sollogoub M. NHC-capped cyclodextrins (ICyDs): insulated metal complexes, commutable multicoordination sphere, and cavity-dependent catalysis. Angewandte Chemie (International Ed. in English). 52: 7213-8. PMID 23733709 DOI: 10.1002/Anie.201301225 |
0.661 |
|
2013 |
Zaborova E, Guitet M, Prencipe G, Blériot Y, Ménand M, Sollogoub M. An "against the rules" double bank shot with diisobutylaluminum hydride to allow triple functionalization of α-cyclodextrin. Angewandte Chemie (International Ed. in English). 52: 639-44. PMID 23172810 DOI: 10.1002/Anie.201204974 |
0.685 |
|
2013 |
Guitet M, Marcelo F, De Beaumais SA, Zhang Y, Jiménez-Barbero J, Tilloy S, Monflier E, Ménand M, Sollogoub M. Diametrically opposed carbenes on an α-cyclodextrin: Synthesis, characterization of organometallic complexes and Suzuki-Miyaura coupling in ethanol and in water European Journal of Organic Chemistry. 3691-3699. DOI: 10.1002/Ejoc.201300190 |
0.715 |
|
2012 |
Guitet M, de Beaumais SA, Blériot Y, Vauzeilles B, Zhang Y, Ménand M, Sollogoub M. Cyclodextrins selectively modified on both rims using an O-3-debenzylative post-functionalisation, a consequence of the Sorrento meeting. Carbohydrate Research. 356: 278-81. PMID 22209379 DOI: 10.1016/J.Carres.2011.12.002 |
0.69 |
|
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