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Original Articles

A Brief Review of the Anticancer Activity of α-Aminophosphonic Acid Derivatives and a Report on the in Vitro Activity of Some Dialkyl α-aryl- (or Heteroaryl)-α-(Diphenylmethylamino)Methanephosphonates

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Pages 1149-1155 | Received 15 Feb 2014, Accepted 21 Feb 2014, Published online: 04 Aug 2014

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Read on this site (6)

Mohamed Hussien, Tarik E. Ali, Ibrahim El-Tantawy El Sayed, Abdelaleem Hassan Abdelaleem & H. M. Torkey. (2023) Ultrasound-assisted construction of novel diethyl {(4-oxo-1,4-dihydroquinolin-3-yl) (aryl/heteroarylamino)methyl}phosphonates using CdI2 nanoparticles as an efficient catalyst: Synthesis, characterization, and antifungal properties. Phosphorus, Sulfur, and Silicon and the Related Elements 198:10, pages 854-865.
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Harry R. Hudson, Ádám Tajti, Erika Bálint, Mátyás Czugler, Konstantin Karaghiosoff & György Keglevich. (2020) Microwave-assisted synthesis of α-aminophosphonates with sterically demanding α-aryl substituents. Synthetic Communications 50:10, pages 1446-1455.
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Jarosław Lewkowski, Rafał Karpowicz, Maria Rodriguez Moya & Beata Pasternak. (2017) Dibenzyl amino(pyren-1-yl)methyl phosphonates—Their NMR and mass spectrometry characterizations. Phosphorus, Sulfur, and Silicon and the Related Elements 192:6, pages 719-726.
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Gerhard Hägele. (2017) Some introductory remarks to “In memoriam of Prof. Harry R. Hudson”. Phosphorus, Sulfur, and Silicon and the Related Elements 192:6, pages 578-580.
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Harry R. Hudson, Mátyás Czugler, Rosalind J. Lee & Thomas M. Woodroffe. (2016) Extremely short H···H distances and intermolecular hydrogen-bonding patterns of dialkyl α-aryl-α-(diphenylmethylamino)methanephosphonates. Phosphorus, Sulfur, and Silicon and the Related Elements 191:3, pages 469-477.
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Harry R. Hudson, Sia N. Koroma & Isaac A. O. Ojo. (2015) The Preparation and Spectroscopic Characterization of Chloroalkyl- and Chlorobenzyl-Aminobis(Methylenephosphonic Acids). Phosphorus, Sulfur, and Silicon and the Related Elements 190:12, pages 2187-2193.
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Articles from other publishers (12)

Edyta Proniewicz & Tomasz K. Olszewski. (2022) SERS/TERS Characterization of New Potential Therapeutics: The Influence of Positional Isomerism, Interface Type, Oxidation State of Copper, and Incubation Time on Adsorption on the Surface of Copper(I) and (II) Oxide Nanoparticles. Journal of Medicinal Chemistry 65:5, pages 4387-4400.
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Mohamed Hussien, Tarik E. Ali, Ibrahim El-Tantawy El Sayed, Abdelaleem Hassan Abdelaleem & H. M. Torkey. (2022) Ultrasound-Promoted Kabachnik–Fields Synthesis of Novel Chromonyl α-Aminophosphonate Derivatives Incorporating Nitrogen Heterocycles Using CdI2 Nanoparticles as an Efficient Catalyst: Evaluation of Their Antifungal Properties. HETEROCYCLES 104:12.
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Hanmant M. Kasralikar. (2021) Nano TiO2/SiO2: An Efficient and Reusable Catalyst for the Synthesis of α-aminophosphonates. International Journal of Advanced Research in Science, Communication and Technology, pages 53-57.
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Muhammad Faisal. 2020. Green Sustainable Process for Chemical and Environmental Engineering and Science. Green Sustainable Process for Chemical and Environmental Engineering and Science 113 139 .
Erika L. Loredo-Calderón, Carlos A. Velázquez-Martínez, Mónica A. Ramírez-Cabrera, Eugenio Hernández-Fernández, Verónica M. Rivas-Galindo, Eder Arredondo Espinoza & Susana T. López-Cortina. (2019) Synthesis of novel α-aminophosphonates under microwave irradiation, biological evaluation as antiproliferative agents and apoptosis inducers. Medicinal Chemistry Research 28:11, pages 2067-2078.
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Tsubasa Inokuma, Takuya Sakakibara, Takatoshi Someno, Kana Masui, Akira Shigenaga, Akira Otaka & Ken‐ichi Yamada. (2019) Asymmetric Synthesis of α‐Amino Phosphonic Acids using Stable Imino Phosphonate as a Universal Precursor. Chemistry – A European Journal 25:60, pages 13829-13832.
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Bo-Hang An, Ru-Fen Zhang, Qian-Li Li, Xiu-Mei Du, Jing Ru, Shao-Liang Zhang & Chun-Lin Ma. (2019) Syntheses, structures and in vitro cytostatic activity of four novel homochiral organotin(IV) phosphonates. Journal of Organometallic Chemistry 881, pages 51-57.
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Kolio D. Troev. 2018. Reactivity of P-H Group of Phosphorus Based Compounds. Reactivity of P-H Group of Phosphorus Based Compounds 291 409 .
Jarosław Lewkowski, Marta Morawska, Rafał Karpowicz, Piotr Rychter, Diana Rogacz, Kamila Lewicka & Piotr Dobrzyński. (2017) Evaluation of ecotoxicological impact of new pyrrole-derived aminophosphonates using selected bioassay battery. Ecotoxicology 26:7, pages 914-929.
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Jarosław Lewkowski, Marta Morawska, Anna Kaczmarek, Diana Rogacz & Piotr Rychter. (2017) Novel N-Arylaminophosphonates Bearing a Pyrrole Moiety and Their Ecotoxicological Properties. Molecules 22:7, pages 1132.
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E. Proniewicz, S. Vantasin, T. K. Olszewski, B. Boduszek & Y. Ozaki. (2017) Biological application of water-based electrochemically synthesized CuO leaf-like arrays: SERS response modulated by the positional isomerism and interface type. Physical Chemistry Chemical Physics 19:47, pages 31842-31855.
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L. I. Vagapova, L. R. Amirova, A. R. Burilov, M. A. Pudovik & O. G. Sinyashin. (2015) Synthesis and structure of new phosphorylated β- and γ-amino acetals containing a sterically hindered phenol group. Russian Journal of Organic Chemistry 51:9, pages 1268-1271.
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