Synthesis of analogs of the C-terminal part of fibrinopeptide A

Abstract

The pyrocarbonate (I) was taken 20% excess and was added to the reaction mixture in the form of a I M solution in acetone. The time and temperature of the reaction was varied according to the reactivity of the amino acid. The Pboc derivatives of the amino acids were isolated by the method generally used in similar cases [5, 6] and were crystallized from the… (More)
DOI: 10.1007/BF00713362

Topics

Cite this paper

@article{Poyarkova2004SynthesisOA, title={Synthesis of analogs of the C-terminal part of fibrinopeptide A}, author={Svetlana A Poyarkova and V. K. Kibirev and S. B. Serebryani}, journal={Chemistry of Natural Compounds}, year={2004}, volume={14}, pages={365-366} }