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Quaternary imine salts, hydrolysis

The asymmetric alkylation of glycine derivatives constitutes a general means of accessing a wide range of natural and unnatural oc-amino acids.111 Recently it has been established that the quaternary ammonium salt, (lS,2S,4S,5/ ,l / )-l-anthracen-9-yl)methyl-2-[benzyloxy(quinolin-4-yl)methyl]-5-ethyl-l-azoniabicyclo [2.2.2]octane bromide, is a highly effective catalyst in the asymmetric liquid-liquid phase-transfer alkylation of tert-butyl AI-(diphenylmethylene)glycinate. Subsequent hydrolysis of the imine provides access to a wide range of a-amino acid fcrt-butyl... [Pg.27]


See other pages where Quaternary imine salts, hydrolysis is mentioned: [Pg.345]    [Pg.778]    [Pg.340]    [Pg.41]    [Pg.271]    [Pg.730]    [Pg.228]    [Pg.1254]    [Pg.730]   
See also in sourсe #XX -- [ Pg.680 ]




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Hydrolysis imine

Imine salts

Imine salts Imines

Imine salts hydrolysis

Imines, hydrolysis

Quaternary salts

Salt hydrolysis

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