Special Issue “Organophosphorus Chemistry: A New Perspective”
Conflicts of Interest
References
- He, R.; Ding, C.; Marouka, K. Phosphonium Salts as Chiral Phase-Transfer Catalysts: Asymmetric Michael and Mannich Reactions of 3-Aryloxindoles. Angew. Chem. 2009, 48, 4559–4561. [Google Scholar] [CrossRef] [PubMed]
- Bradaric, C.J.; Downard, A.; Kennedy, C.; Robertson, A.J.; Zhou, Y. Industrial preparation of phosphonium ionic liquids. Green Chem. 2003, 5, 143–152. [Google Scholar] [CrossRef]
- Allen, D.W.; Loakes, D.; Tebby, J. Organophosphorus Chemistry; The Royal Society of Chemistry: London, UK, 2016; Volume 45. [Google Scholar] [CrossRef] [Green Version]
- Maryanoff, B.E.; Reitz, A.B. The Wittig olefination reaction and modifications involving phosphoryl-stabilized carbanions. Stereochemistry, mechanism, and selected synthetic aspects. Chem. Rev. 1989, 89, 863–927. [Google Scholar] [CrossRef]
- Kolodiazhnyi, O.I. Phosphorus Compounds of Natural Origin: Prebiotic, Stereochemistry, Application. Symmetry 2021, 13, 889. [Google Scholar] [CrossRef]
- Russell, R.G.G. Bisphosphonates: The first 40 years. Bone 2011, 49, 2. [Google Scholar] [CrossRef]
- Caminade, A.-M. Phosphorus Dendrimers as Nanotools against Cancers. Molecules 2020, 25, 3333. [Google Scholar] [CrossRef]
- Adamek, J.; Grymel, M.; Kuźnik, A.; Październiok-Holewa, A. 1-Aminoalkylphosphonium Derivatives: Smart Synthetic Equivalents of N-Acyliminium-Type Cations, and Maybe Something More: A Review. Molecules 2022, 27, 1562. [Google Scholar] [CrossRef]
- Grymel, M.; Lalik, A.; Kazek-Kęsik, A.; Szewczyk, M.; Grabiec, P.; Erfurt, K. Design, Synthesis and Preliminary Evaluation of the Cytotoxicity and Antibacterial Activity of Novel Triphenylphosphonium Derivatives of Betulin. Molecules 2022, 27, 5156. [Google Scholar] [CrossRef] [PubMed]
- Kuźnik, A.; Kozicka, D.; Hawranek, W.; Socha, K.; Erfurt, K. One-Pot and Catalyst-Free Transformation of N-Protected 1-Amino-1-Ethoxyalkylphosphonates into Bisphosphonic Analogs of Protein and Non-Protein α-Amino Acids. Molecules 2022, 27, 3571. [Google Scholar] [CrossRef] [PubMed]
- Vassaki, M.; Lazarou, S.; Turhanen, P.; Choquesillo-Lazarte, D.; Demadis, K.D. Drug-Inclusive Inorganic–Organic Hybrid Systems for the Controlled Release of the Osteoporosis Drug Zoledronate. Molecules 2022, 27, 6212. [Google Scholar] [CrossRef]
- Kukkonen, E.; Virtanen, E.J.; Moilanen, J.O. α-Aminophosphonates, -Phosphinates, and -Phosphine Oxides as Extraction and Precipitation Agents for Rare Earth Metals, Thorium, and Uranium: A Review. Molecules 2022, 27, 3465. [Google Scholar] [CrossRef] [PubMed]
- Brol, A.; Olszewski, T.K. Deamination of 1-Aminoalkylphosphonic Acids: Reaction Intermediates and Selectivity. Molecules 2022, 27, 8849. [Google Scholar] [CrossRef] [PubMed]
- del Corte, X.; Maestro, A.; López-Francés, A.; Palacios, F.; Vicario, J. Synthesis of Tetrasubstituted Phosphorus Analogs of Aspartic Acid as Antiproliferative Agents. Molecules 2022, 27, 8024. [Google Scholar] [CrossRef] [PubMed]
- Chmielewska, E.; Miodowska, N.; Dziuk, B.; Psurski, M.; Kafarski, P. One-Pot Phosphonylation of Heteroaromatic Lithium Reagents: The Scope and Limitations of Its Use for the Synthesis of Heteroaromatic Phosphonates. Molecules 2023, 28, 3135. [Google Scholar] [CrossRef] [PubMed]
- Janicki, I.; Kiełbasiński, P. Highly Z-Selective Horner–Wadsworth–Emmons Olefination Using Modified Still–Gennari-Type Reagents. Molecules 2022, 27, 7138. [Google Scholar] [CrossRef] [PubMed]
- Koprowski, M.; Owsianik, K.; Knopik, Ł.; Vivek, V.; Romaniuk, A.; Różycka-Sokołowska, E.; Bałczewski, P. Comprehensive Review on Synthesis, Properties, and Applications of Phosphorus (PIII, PIV, PV) Substituted Acenes with More Than Two Fused Benzene Rings. Molecules 2022, 27, 6611. [Google Scholar] [CrossRef] [PubMed]
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content. |
© 2023 by the author. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Share and Cite
Adamek, J. Special Issue “Organophosphorus Chemistry: A New Perspective”. Molecules 2023, 28, 4752. https://doi.org/10.3390/molecules28124752
Adamek J. Special Issue “Organophosphorus Chemistry: A New Perspective”. Molecules. 2023; 28(12):4752. https://doi.org/10.3390/molecules28124752
Chicago/Turabian StyleAdamek, Jakub. 2023. "Special Issue “Organophosphorus Chemistry: A New Perspective”" Molecules 28, no. 12: 4752. https://doi.org/10.3390/molecules28124752