Synthesis and investigation of compounds with potential biological activity. IV. Synthesis of pteroyl-d, L-γ-fluorglutamic acid

Abstract

Pteroyl-D, L-γ-fluorglutamic acid was synthesized by a triple condensation of 2,4,5-triamino-6-oxypyrimidine with α,β-dibromopropionic aldehyde and n-aminobenzoyl-D, L-γ-fluorglutamic acid in an aqueous alcoholic medium at pH 3.0–4.0.

DOI: 10.1007/BF00759633

Cite this paper

@article{Alekseeva2004SynthesisAI, title={Synthesis and investigation of compounds with potential biological activity. IV. Synthesis of pteroyl-d, L-γ-fluorglutamic acid}, author={L. V. Alekseeva and N. L. Burde and Bj{\"{o}rn Lundin}, journal={Pharmaceutical Chemistry Journal}, year={2004}, volume={2}, pages={557-558} }