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Enantioselective synthesis of -amino acid
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New optically active bis-quaternary ammonium salts were synthesized and applied to catalytic asymmtric alkylation of tert-butyl glycinate benzophenone Schiff base to provide a chiral α-amino acid derivative with 54% ee.
3p
giesumanh
13-11-2018
22
1
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Phase-transfer-catalyzed alkylation of glycinate Schiff base with racemic secondary alkyl halides proceeded with excellent levels of synand enantioselectivities under the influence of a chiral quaternary ammonium bromide and 18- crown-6. The alkylation product can be selectively converted to the corresponding anti isomer, allowing the preparation of all the stereoisomers of β-alkyl-α-amino acid derivatives.
12p
heoxinhkute
19-07-2010
81
5
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