Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Pyranoside ligands

Fig. 21. Detail of the monosaccharide binding pocket with (left) pyranoside ligand 237 and (right) septanoside ligand 208 as determined from the QM/MM computations (taken from ref. 124). Fig. 21. Detail of the monosaccharide binding pocket with (left) pyranoside ligand 237 and (right) septanoside ligand 208 as determined from the QM/MM computations (taken from ref. 124).
Over the years, several authors have developed new diphosphite ligands with binaphthyl, spiro, pyranoside, and macrocyclic backbones for asymmetric hydroformylation of vinyl arenes with low-to moderate success (ee s from 36% to 76%) [48-58]. [Pg.56]

Mazuela, J. Norrby, P. O. Andersson, P. G. Ramies, O. Dieguez, M. Pyranoside phosphite-oxazoline ligands for the highly versatile and enanti-oselective Ir-catalyzed hydrogenation of minimally functionalized olefins. A combined theoretical and experimental study. /. Am. Chem. Soc. 2011,133, 13634-13645. [Pg.131]

See other pages where Pyranoside ligands is mentioned: [Pg.973]    [Pg.973]    [Pg.974]    [Pg.974]    [Pg.975]    [Pg.976]    [Pg.178]    [Pg.34]    [Pg.973]    [Pg.973]    [Pg.974]    [Pg.974]    [Pg.975]    [Pg.976]    [Pg.178]    [Pg.34]    [Pg.335]    [Pg.246]    [Pg.977]    [Pg.172]    [Pg.173]    [Pg.174]    [Pg.174]    [Pg.455]    [Pg.431]    [Pg.447]    [Pg.180]    [Pg.304]    [Pg.1011]    [Pg.1013]    [Pg.1020]    [Pg.1113]    [Pg.1115]    [Pg.1116]    [Pg.2337]    [Pg.163]    [Pg.242]    [Pg.610]    [Pg.41]    [Pg.148]    [Pg.292]    [Pg.95]    [Pg.444]    [Pg.33]    [Pg.388]    [Pg.135]    [Pg.57]    [Pg.254]    [Pg.908]   
See also in sourсe #XX -- [ Pg.178 ]



SEARCH



Pyranoside

Pyranosides

© 2024 chempedia.info