https://orcid.org/0000-0003-1715-5095
References
- Metcalf, W.-W.; Van Der Donk, W.-A. Biosynthesis of Phosphonic and Phosphinic Acid Natural Products. Annu. Rev. Biochem. 2009, 78, 65–94. DOI: 10.1146/annurev.biochem.78.091707.100215.
- Horsman, G.-P.; Zechel, D.-L. Phosphonate Biochemistry. Chem. Rev. 2017, 117, 5704–5783. DOI: 10.1021/acs.chemrev.6b00536.
- Kafarski, P.; Lejczak, B. Aminophosphonic Acids of Potential Medical Importance. Curr. Med. Chem. Anticancer. Agents. 2001, 1, 301–312. DOI: 10.2174/1568011013354543.
- Zhou, C.; Luo, X.; Chen, N.; Zhang, L.; Gao, J. C–P Natural Products as Next- Generation Herbicides: chemistry and Biology of Glufosinate. J. Agric. Food Chem. 2020, 68, 3344–3353. DOI: 10.1021/acs.jafc.0c00052.
- Takeuchi, M.; Nakajima, M.; Ogita, T.; Inukai, M.; Kodama, K.; Furuya, K.; Nagaki, H.; Haneishi, T. Fosfonochlorin, a New Antibiotic with Spheroplast Forming Activity. J. Antibiot. (Tokyo) 1989, 42, 198–202. DOI: 10.7164/antibiotics.42.198.
- Warren, W.-A. Biosynthesis of Phosphonic Acids in Tetrahymena. Biochim. Biophys. Acta 1968, 156, 340–346. DOI: 10.1016/0304-4165(68)90263-8.
- Seidel, H.-M.; Freeman, S.; Seto, H.; Knowles, J.-R. Phosphonate Biosynthesis: isolation of the Enzyme Responsible for the Formation of a Carbon-Phosphorus Bond. Nature 1988, 335, 457–458. DOI: 10.1038/335457a0.
- Kayrouz, C. M.; Zhang, Y.; Pham, T. M.; Ju, K.-S. Genome Mining Reveals the Phosphonoalamide Natural Products and a New Route in Phosphonic Acid Biosynthesis. ACS Chem. Biol. 2020, 15, 1921–1929. DOI: 10.1021/acschembio.0c00256.
- Gama, S.-R.; Stankovic, T.; Hupp, K. Biosynthesis of the Fungal Organophosphonate Fosfonochlorin Involves an Iron (II) and 2-(Oxo) Glutarate Dependent Oxacyclase. ChemBioChem. 2021, 58, 326–329. DOI: 10.1002/cbic.202100352.
- Ghomri, A.; Atmani, A. Synthesis of Phosphoenol Pyruvates. Theoretical and Experimental Study. C. R. Chim. 2014, 17, 1230–1236. DOI: 10.1016/j.crci.2014.03.005.
- Cao, Y.; Gao, Z.; Li, J.; Bi, X.; Yuan, L.; Pei, C.; Guo, Y.; Shi, E. Regioselective O/C Phosphorylation of α-Chloroketones: A General Method for the Synthesis of Enol Phosphates and β-Ketophosphonates via Perkow/Arbuzov Reaction. RSC Adv. 2020, 10, 29493–29497. DOI: 10.1039/D0RA05140C.
- Ferao, A.-E. Reaction of Chloroacetone with Trimethylphosphite: Perkow versus Michaelis-Arbuzov Reaction Paths. J. Phys. Chem. A 2017, 121, 6517–6522. DOI: 10.1021/acs.jpca.7b06262.