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Asymmetric catalysis privileged ligands

In large-scale processes, a limited number of phosphines and phosphites are used, which can be called, in analogy to ligands in asymmetric catalysis, privileged hgands. Somewhat more variants are available from commercial suppliers. [Pg.77]

Li H, Chen YG, Deng L (2011) Cinchona Alkaloids. In Zhou QL (ed) Privileged Catalysts and Ligands in Asymmetric Catalysis. Wiley-VCH, Weinheim, p 361... [Pg.160]

Oxazolines are nowadays essential ligands in asymmetric catalysis and also important synthons for stereoselective synthesis [8]. The success of the Cj-symmetric bis(oxazolines) ( BOX ) and pyridine-bis(oxazolines) ( Pybox ) discovered in the early 1990s has established them as a privileged class of ligands [9]. In contrast, the development and application of trisoxazolines lagged behind for a long time. Katsuki and collaborators [10] reported the first example of a chiral trisoxazoline in 1995 and their use in the allylic oxidation of alkenes (Kharasch-Sosnovsky reaction), as well as the enantioselective addition of diethylzinc to aldehydes. [Pg.314]

Teichert JF, Feringa BL (2010) Phosphoramidites privileged ligands in asymmetric catalysis. [Pg.37]


See other pages where Asymmetric catalysis privileged ligands is mentioned: [Pg.170]    [Pg.248]    [Pg.118]    [Pg.146]    [Pg.73]    [Pg.557]    [Pg.66]    [Pg.92]    [Pg.150]    [Pg.206]    [Pg.2]    [Pg.561]    [Pg.344]    [Pg.355]    [Pg.313]    [Pg.337]    [Pg.207]   
See also in sourсe #XX -- [ Pg.561 , Pg.562 ]




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