Synthesis of 2-amino acids via selective mono-N-alkylation of trichloroacetamide by 2-bromo carboxylic esters under solid-liquid phase-transfer catalysis conditions

D Albanese, D Landini, M Penso

Index: Albanese, Domenico; Landini, Dario; Penso, Michele Journal of Organic Chemistry, 1992 , vol. 57, # 5 p. 1603 - 1605

Full Text: HTML

Citation Number: 21

Abstract

In a previous paper'we described a new procedure for the synthesis of 2-amino acids 6 via N- alkylation of trifluoroacetamide (1) with 2-bromo carboxylic esters 3 under solid-liquid phase- transfer catalysis (SL-PTC) conditions, followed by hydrolysis of the intermediate N- (trifluoroacetyl)-2-amino esters 4 (Scheme I). The use of an excess of Wuoroacetamide (I), which cannot be recovered at the end of the reaction, and its relatively high cost are ...

Related Articles:

Aminosäuren, I. Darstellung von Aminosäuren aus Halogencarbonsäure??Alkylestern mit Alkalimetallcyanaten1)

[Effenberger, Franz; Drauz, Karlheinz; Foerster, Siegfried; Mueller, Wolfgang Chemische Berichte, 1981 , vol. 114, # 1 p. 173 - 189]

Synthesis of 2-amino acids via selective mono-N-alkylation of trichloroacetamide by 2-bromo carboxylic esters under solid-liquid phase-transfer catalysis conditions

[Journal of Organic Chemistry, , vol. 57, # 5 p. 1603 - 1605]

Transkarbams as transdermal permeation enhancers: effects of ester position and ammonium carbamate formation

[Bioorganic and Medicinal Chemistry Letters, , vol. 20, # 9 p. 2726 - 2728]

More Articles...