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Pisaneschi, F., Lin, Y.H., Leonard, P.G., Satani, N., Yan, V.C., Hammoudi, N., Raghavan, S., Todd, M., Link, K., Georgiou, D., Czako, B. and Muller, F. (2019) The 3S Enantiomer Drives Enolase Inhibitory Activity in SF2312 and Its Analogues. Molecules, 24, 2510-2516.
https://doi.org/10.3390/molecules24132510

has been cited by the following article:

• TITLE: An Aminopyrrolidinyl Phosphonates—A New Class of Antibiotics: Facile Synthesis and Predicted Biological Activity

  AUTHORS: Abed Al Aziz Al Quntar, Hasan Dweik, Ahmad Jabareen, Tatyana A. Gloriozova, Valery M. Dembitsky

  KEYWORDS: Alkynylphosphonates, Cyclization, Pyrrolidine, β-Aminophosphonates, Amine Addition, Antibiotics

  JOURNAL NAME: International Journal of Organic Chemistry, Vol.10 No.4, December 29, 2020

  ABSTRACT: A novel class of aminopyrrolidinyl phosphonates was synthesized in 74% - 80% isolated yield by the addition of three-fold excess of primary amines to diethyl 4-chloro-1-butynylphosphonates. The reaction was carried out at room temperature and in the absence of solvent or catalyst to give solely compounds which showed predicted biological activity based on PASS program. Some of the synthesized derivatives of antibiotics exhibit properties for the treatment of stroke, the treatment of acute neurological disorders, and can also be acetyl esterase inhibitors.