On the selectivity of acylation of unprotected diamino acids
- 1 April 1968
- journal article
- research article
- Published by Canadian Science Publishing in Canadian Journal of Chemistry
- Vol. 46 (7) , 1047-1051
- https://doi.org/10.1139/v68-177
Abstract
P-Nitrophenyl acetate and other esters except formates, will acylate the unprotected diamino acids homolysine, lysine, and ornithine, exclusively at the ω-amino group at pH 11. At lower alkaline pH's, the reaction is preferential but not selective. The reaction with diaminobutyric acid and diaminopropionic acid is not selective at any alkaline pH. ε-N-Acetyllysine can be prepared directly by the action of excess phenyl acetate on lysine at pH 11.This publication has 2 references indexed in Scilit:
- Quantitative studies of the avidity of naturally occurring substances for trace metals. 2. Amino-acids having three ionizing groupsBiochemical Journal, 1952
- The availability of the acetyl derivatives of lysine for growthBiochemical Journal, 1943