1638884-72-6Relevant articles and documents
Phosgene-free synthesis of polypeptides using activated urethane derivatives of α-amino acids: An efficient synthetic approach to hydrophilic polypeptides
Yamada, Shuhei,Sudo, Atsushi,Goto, Mitsuaki,Endo, Takeshi
, p. 29890 - 29896 (2014)
A series of polypeptides have been synthesized from the corresponding N-phenoxycarbonyl derivatives of hydroxyl- or amino-functionalized α-amino acids such as l-serine, l-cysteine, l-threonine, l-tyrosine, l-glutamine, and l-asparagine. These derivatives are prepared by N-carbamylation of tetrabutylammonium salts of α-amino acids with diphenyl carbonate (DPC). The synthesis of polypeptides can be achieved by heating these N-phenoxycarbonyl derivatives at 60 °C in N,N-dimethylacetamide (DMAc) in the presence of n-butylamine through the polycondensation of the derivatives with accompanying elimination of phenol and CO2. The NMR and MALDI-TOF mass analyses of the resulting polypeptides revealed that n-butylamine was successfully incorporated into the chain end of the polypeptides. Molecular weights of the polypeptides were controlled by varying the feed ratio of the urethane derivatives to n-butylamine. The employment of an amine-terminated poly(ethylene glycol) in place of n-butylamine permitted the successful synthesis of the corresponding diblock copolymers composed of polyether and polypeptide segments.
