Go to content
UR Home

Research on the mechanism of action of local anesthetics. Part 7: Synthesis of N-aminoacyl-2,6-dimethylaniline, - benzylamine and -2-phenylethylamine enantiomers

Schönenberger, Helmut ; Endres, W.


N-Phthaloyl amino acids were converted by PCl5 into their acid chlorides, which were used to acylate RNH2 (I, R = 2,6-Me2C6H3, PhCH2, and PhCH2CH2) and the amides were hydrazinolyzed to remove the protective group and give D- and L-H2NCHR1CONHR (R as in I, R1 = Me, Me2CH, Me2CHCH2, PhCH2).

Owner only: item control page
  1. Homepage UR

University Library

Publication Server


Publishing: oa@ur.de

Dissertations: dissertationen@ur.de

Research data: daten@ur.de

Contact persons