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Chiral Recognition Using Modified Cyclodextrins

Chirality of derivatized cyclodextrin was used for recognition of stereoisomers. Phenylazobenzoyl modified y-cyclodextrin was anchored onto silica gel used as stationary phase in HPLC and photoresponsive chromatographic behavior of dansyl amino acid enantiomers was studied [64],... [Pg.215]

Reetz et al. prepared /3-cyclodextrin-modified diphosphine 18 and a series of derivatives by phosphinomethylation of the corresponding amino-substituted cyclodextrin precursors [25], The ligands were used in biphasic hydroformylation of 1-octene and competitive hydrogenation of 1-alkenes, with rather poor results. The chiral cavity in the backbone might achieve molecular recognition of certain pro-chiral substrates and thus provide enantioselectivity in the products. [Pg.183]


See other pages where Chiral Recognition Using Modified Cyclodextrins is mentioned: [Pg.299]    [Pg.1037]    [Pg.183]    [Pg.721]    [Pg.353]    [Pg.219]    [Pg.130]    [Pg.329]    [Pg.59]    [Pg.150]    [Pg.59]    [Pg.73]    [Pg.342]    [Pg.342]    [Pg.1768]   


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Chiral modifiers

Chiral recognition

Chirality modifiers

Chirality recognition

Cyclodextrin modified

Cyclodextrin use

Cyclodextrins using

Cyclodextrins, chiral recognition

Modified cyclodextrins

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