�ber die Geschwindigkeit der Aminolyse von verschiedenen neuen, aktivierten, N-gesch�tzten ?-Aminos�ure-phenylestern, insbesondere 2,4,5-Trichlorphenylestern
作者:J. Pless、R. A. Boissonnas
DOI:10.1002/hlca.19630460516
日期:——
A comparison of the ate of aminolysis of many substituted phenyl esters of N-protected α-amino-acids shows that the 2,4,5-trichlorophenyl esters are promising new active derivatives for the synthesis of peptides.
Novel polyfunctional small amphiphilic peptide dendrimers characterized by incorporation of a new core compounds - tris-amino acids or tetrakis-amino alcohols that originated from a series of basic amino acids - were efficiently synthesized. These new core elements yielded molecules with multiple branching and (+5)/(+6) charge at the 1-st dendrimer generation. Dendrimers exhibited significant antimicrobial
Analogs of enkephalin having agonist activity at opiate receptors are disclosed herein. These analogs are useful as analgesics, non-addicting narcotic antagonists and anti-diarrheal agents.