https://m2.mtmt.hu/ eng 2026-06-25 16:27 BookChapter 36843128 APPROVED true 0 false 2026-03-03T14:26:35.447+0000 2026-03-03T13:59:04.257+0000 2026-01-03T16:40:01.256+0000 true 10030275 Bálint Erika /api/author/10030275 Author Erika Bálint (Szerves kémia) true 10030275 2026-03-03T13:59:04.183+0000 false false true 25 25 /api/publicationtype/25 PublicationType Chapter in Book 2 true 25 BookChapter true 10000398 Chapter true 25 25 /api/publicationtype/25 PublicationType Chapter in Book 2 true 25 BookChapter /api/subtype/10000398 Könyvfejezet SubType Chapter (Chapter in Book) 220 true 10000398 true 1 /api/category/1 Category Scientific true 1 Chachlaki, Elpiniki 25 46 25 22 2026 true 2026 true true true false false false NONE 2026-03-03 false 0 0 0 0 0 0 0 0 0 0 0 0 2 2 false false false false 2026-04-03T15:40:07.264+0000 6 7 0 2 0 true true 10002 English /api/language/10002 Angol Language English true 2 false true 18501 true 10023 /api/country/10023 Country Netherlands true 19 /api/city/18501 City Amszterdam, Netherlands true true 10483 true 10175 /api/country/10175 Country United Kingdom / England true 2151760 /api/city/10483 City London, United Kingdom / England true 1022850 true 14686 true 10017 /api/country/10017 Country United States of America true 13 /api/city/14686 City Cambridge (MA), United States of America true 10005908 true 30258574 /api/publicationidentifier/30258574 https://doi.org/10.1016/C2024-0-00017-3 10.1016/C2024-0-00017-3 PublicationIdentifier DOI: 10.1016/C2024-0-00017-3 true 6 DOI https://doi.org/@@@ /api/publicationsource/6 DOI PlainSource DOI true true 10001 /api/publicationsourcetype/10001 PublicationSourceType DOI true true 6 true false true 30258573 /api/publicationidentifier/30258573 https://www.worldcat.org/search?q=isbn%3A9780443333743 9780443333743 PublicationIdentifier ISBN: 9780443333743 true 122 ISBN https://www.worldcat.org/search?q=isbn%3A@@@ /api/publicationsource/122 ISBN PlainSource ISBN true true 10002 /api/publicationsourcetype/10002 PublicationSourceType Egyéb true false 122 true false /api/publication/36468792 Demadis Konstantinos D.. Phosphonate Chemistry, Technology, and Applications: Synthesis, Chemistry, and Biomedical Applications. (2026) ISBN:9780443333743 true true 23 23 /api/publicationtype/23 PublicationType Book 3 true 23 Book false false 36468792 false true false true true 10000201 Monograph true 23 23 /api/publicationtype/23 PublicationType Book 3 true 23 Book /api/subtype/10000201 Szakkönyv SubType Monograph (Book) 337 true 10000201 true Book 2026 true 1 /api/category/1 Category Scientific true 1 false Language 10002 /api/language/10002 English Angol English true 2 true PersonAuthorship 132542959 /api/authorship/132542959 Chachlaki, Elpiniki 1 0.5 true false false Chachlaki Elpiniki true false false AuthorshipType 1 /api/authorshiptype/1 Author 0 true 0 true false true PersonAuthorship 132542960 /api/authorship/132542960 Demadis, Konstantinos D. 2 0.5 false true false Demadis Konstantinos D. true false false AuthorshipType 1 /api/authorshiptype/1 Author 0 true 0 true false true PublicationIdentifier 31121362 /api/publicationidentifier/31121362 DOI: 10.1016/B978-0-443-33374-3.00024-4 PlainSource 6 /api/publicationsource/6 DOI PublicationSourceType 10001 /api/publicationsourcetype/10001 DOI true true true DOI DOI https://doi.org/@@@ true true 6 true IDENTICAL 10.1016/B978-0-443-33374-3.00024-4 https://doi.org/10.1016/B978-0-443-33374-3.00024-4 false true PublicationIdentifier 31569226 /api/publicationidentifier/31569226 Scopus: 105027204208 PlainSource 3 /api/publicationsource/3 Scopus PublicationSourceType 10003 /api/publicationsourcetype/10003 Indexelő adatbázis false true true Scopus Scopus http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-@@@ true true 3 true 105027204208 http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-105027204208 false true PublicationIdentifier 31121363 /api/publicationidentifier/31121363 Other URL: https://linkinghub.elsevier.com/retrieve/pii/B9780443333743000244 PlainSource 40 /api/publicationsource/40 Other URL PublicationSourceType 10006 /api/publicationsourcetype/10006 Link true true true Egyéb URL Other URL @@@ true true 40 true IDENTICAL https://linkinghub.elsevier.com/retrieve/pii/B9780443333743000244 https://linkinghub.elsevier.com/retrieve/pii/B9780443333743000244 false true Reference 71151475 /api/reference/71151475 1. Horiguchi 1959: Isolation of 2-Aminoethane phosphonic acid from rumen protozoa., Nature, 184, p. 901, DOI: 10.1038/184901b0 1 10.1038/184901b0 false true Reference 71151476 /api/reference/71151476 2. Stavgianoudaki 2012: Structural diversity in metal phosphonate frameworks: impact on applications.Metal phosphonate chemistry: from synthesis to applications, p. 438 2 false true Reference 71151477 /api/reference/71151477 3. Eicher 2012: The Chemistry of Heterocycles 3 false true Reference 71151478 /api/reference/71151478 4. Pozharskii 2011: Heterocycles in life and society 4 false true Reference 71151479 /api/reference/71151479 5. Balint 2021: Microwave-assisted multicomponent syntheses of heterocyclic phosphonates., Chem Proc, 3, p. 108 5 false true Reference 71151480 /api/reference/71151480 6. Volkova 2023: Synthesis of phosphorus(V)-substituted six-membered N-heterocycles: recent progress and challenges., Molecules, 28, p. 2472, DOI: 10.3390/molecules28062472 6 10.3390/molecules28062472 false true Reference 71151481 /api/reference/71151481 7. Zoń 2012: Synthesis of phosphonic acids and their esters as possible substrates for reticular chemistry.Metal phosphonate chemistry: from synthesis to applications, p. 170 7 false true Reference 71151482 /api/reference/71151482 8. Demmer 2011: Review on modern advances of chemical methods for the introduction of a phosphonic acid group., Chem Rev, 111, p. 7981, DOI: 10.1021/cr2002646 8 10.1021/cr2002646 false true Reference 71151483 /api/reference/71151483 9. Sevrain 2017: Phosphonic acid: preparation and applications., Beilstein J Org Chem, 13, p. 2186, DOI: 10.3762/bjoc.13.219 9 10.3762/bjoc.13.219 false true Reference 71151484 /api/reference/71151484 10. Debrouwer 2019: Methods for the introduction of the phosphonate moiety into complex organic molecules.Organophosphorus chemistry: from molecules to applications, p. 249 10 false true Reference 71151485 /api/reference/71151485 11. Vu 2010: The Michaelis–Becker reaction in phosphonium and imidazolium ionic liquids., Phosphorus Sulfur Silicon, 185, p. 1845, DOI: 10.1080/10426500903329252 11 10.1080/10426500903329252 false true Reference 71151486 /api/reference/71151486 12. Abdel-Rahman 2016: Methods for synthesis of N-heterocyclyl/heteroaryl-α-aminophosphonates and α-(azaheterocyclyl)phosphonates., ARKIVOC, p. 183, DOI: 10.3998/ark.5550190.p009.519 12 10.3998/ark.5550190.p009.519 false true Reference 71151487 /api/reference/71151487 13. Bálint 2018: Synthesis of α-aminophosphonates by the Kabachnik–Fields reaction and by the Pudovik reaction.Organophosphorus chemistry, p. 108 13 false true Reference 71151488 /api/reference/71151488 14. Ordonez 2008: An overview of stereoselective synthesis of a-aminophosphonic., Tetrahedron, 65, p. 17, DOI: 10.1016/j.tet.2008.09.083 14 10.1016/j.tet.2008.09.083 false true Reference 71151489 /api/reference/71151489 15. Wang 2010: Pudovik reaction.Comprehensive organic name reactions and reagents, p. 2280 15 false true Reference 71151490 /api/reference/71151490 16. Haji 2016: Multicomponent reactions: a simple and efficient route to heterocyclic phosphonates., Beilstein J Org Chem, 12, p. 1269, DOI: 10.3762/bjoc.12.121 16 10.3762/bjoc.12.121 false true Reference 71151491 /api/reference/71151491 17. Cherkasov 1998: The Kabachnik-Fields reaction: synthetic potential and the problem of the mechanism., Russ Chem Rev, 65, p. 857, DOI: 10.1070/RC1998v067n10ABEH000421 17 10.1070/RC1998v067n10ABEH000421 false true Reference 71151492 /api/reference/71151492 18. Huisgen 1963: 1,3-Dipolar cycloadditions past and future., Angew Chem Intl Ed, 2, p. 565, DOI: 10.1002/anie.196305651 18 10.1002/anie.196305651 false true Reference 71151493 /api/reference/71151493 19. Shibata 2013: Asymmetric cycloaddition reactions.Comprehensive inorganic chemistry II, p. 249 19 false true Reference 71151494 /api/reference/71151494 20. Sackus 2022: Four-membered rings with three heteroatoms with at least one oxygen, sulfur or nitrogen atom.Comprehensive heterocyclic chemistry IV, p. 648 20 false true Reference 71151495 /api/reference/71151495 21. Kumar 2016: Cheletropic reactions and 1,3-dipolar cycloadditions.Pericyclic reactions, p. 231 21 false true Reference 71151496 /api/reference/71151496 22. Gutierrez 2007: Dealkylation of phosphonate esters with chlorotrimethylsilane., Nucleosides Nucleotides Nucleic Acids, 20, p. 1299, DOI: 10.1081/NCN-100002541 22 10.1081/NCN-100002541 false true Reference 71151497 /api/reference/71151497 23. Chernyshov 2022: Nitrogen-containing heterocyclic compounds obtained from monoterpenes or their derivatives: synthesis and properties., Top Curr Chem, 380, p. 42, DOI: 10.1007/s41061-022-00399-1 23 10.1007/s41061-022-00399-1 false true Reference 71151498 /api/reference/71151498 24. Mayorquín-Torres 2024: Synthetic methods for azaheterocyclic phosphonates and their biological activity: an update 2004−2024., Chem Rev, 124, p. 7907, DOI: 10.1021/acs.chemrev.4c00090 24 10.1021/acs.chemrev.4c00090 false true Reference 71151499 /api/reference/71151499 25. Agami 2002: An efficient asymmetric synthesis of azetidine 2-phosphonic acids., Tetrahedron Lett, 43, p. 4633, DOI: 10.1016/S0040-4039(02)00868-7 25 10.1016/S0040-4039(02)00868-7 false true Reference 71151500 /api/reference/71151500 26. Kaboudin 2013: A novel and simple method for the preparation of (R)- and (S)-pyrrolidine-2-phosphonic acids: phosphonic acid analogues of proline., Tetrahedron Asymmetry, 24, p. 1562, DOI: 10.1016/j.tetasy.2013.10.013 26 10.1016/j.tetasy.2013.10.013 false true Reference 71151501 /api/reference/71151501 27. Kozachkova 2020: Interaction between 2-pyrrolidine-1-hydroxymethane-1,1-diphosphonic acid and palladium(II) in aqueous solutions., Inorg Chim Acta, 505, p. 119503, DOI: 10.1016/j.ica.2020.119503 27 10.1016/j.ica.2020.119503 false true Reference 71151502 /api/reference/71151502 28. Hossain 2018: A review on heterocyclic: synthesis and their application in medicinal chemistry of imidazole moiety., Sci J Chem, 6, p. 83, DOI: 10.11648/j.sjc.20180605.12 28 10.11648/j.sjc.20180605.12 false true Reference 71151503 /api/reference/71151503 29. Budnyak 2018: Imidazole-2yl-phosphonic acid derivative grafted onto mesoporous silica surface as a novel highly effective sorbent for uranium(VI) ion extraction., ACS Appl Mater Interfaces, 10, p. 6681, DOI: 10.1021/acsami.7b17594 29 10.1021/acsami.7b17594 false true Reference 71151504 /api/reference/71151504 30. Boduszek 2002: Synthesis of new imidazole aminophosphonic and aminophosphinic acids., Pol J Chem, p. 1619 30 false true Reference 71151505 /api/reference/71151505 31. Reid 2020: Zoledronate., Bone, 137, p. 115390, DOI: 10.1016/j.bone.2020.115390 31 10.1016/j.bone.2020.115390 false true Reference 71151506 /api/reference/71151506 32. Ratrout 2014: Efficient synthesis of zoledronic acid starting from ter-butyl imidazol-1-yl acetate., Pharm Chem J, 48, p. 837 32 false true Reference 71151507 /api/reference/71151507 33. Zhou 2012: Recent researches in triazole compounds as medicinal drugs., Curr Med Chem, 19, p. 239, DOI: 10.2174/092986712803414213 33 10.2174/092986712803414213 false true Reference 71151508 /api/reference/71151508 34. Zhai 2013: Crystal transformation synthesis of a highly stable phosphonate MOF for selective adsorption of CO2., CrystEngComm, 15, p. 2040, DOI: 10.1039/C2CE26701B 34 10.1039/C2CE26701B false true Reference 71151509 /api/reference/71151509 35. Chachlaki 2022: 5-Phenyl-3-(2-phosphonoethyl)-1,2,3-triazol-1-ium., IUCrData, 7, p. x220189, DOI: 10.1107/S2414314622001894 35 10.1107/S2414314622001894 false true Reference 71151510 /api/reference/71151510 36. Svintsitskaya 2014: Stereo- and regioselective synthesis of β-amino-β-tetrazolylvinylphosphonates., Tetrahedron Lett, 55, p. 5381, DOI: 10.1016/j.tetlet.2014.08.018 36 10.1016/j.tetlet.2014.08.018 false true Reference 71151511 /api/reference/71151511 37. Naylor 1985: The antiviral activity of tetrazole phposphonic acids and their analogues., Nucleic Acids Res, 13, p. 8519, DOI: 10.1093/nar/13.23.8519 37 10.1093/nar/13.23.8519 false true Reference 71151512 /api/reference/71151512 38. Buffat 2004: Synthesis of piperidines., Tetrahedron, 60, p. 1701, DOI: 10.1016/j.tet.2003.11.043 38 10.1016/j.tet.2003.11.043 false true Reference 71151513 /api/reference/71151513 39. Rabasso 2006: Synthesis of a-amino tetrahydropyranyl-, tetrahydrothiopyranyl-,4- and 3-piperidinyl-phosphonic acids via phosphite addition to iminium ions., Tetrahedron, 62, p. 7445, DOI: 10.1016/j.tet.2006.05.016 39 10.1016/j.tet.2006.05.016 false true Reference 71151514 /api/reference/71151514 40. Taddei 2001: New hybrid zirconium aminophosphonates containing piperidine and bipiperidine groups., Inorg Chem, 50, p. 10835, DOI: 10.1021/ic201381t 40 10.1021/ic201381t false true Reference 71151515 /api/reference/71151515 41. Redmore 1970: Phosphorus derivatives of nitrogen heterocycles. 2. Pyridinephosphonic acid derivatives., J Org Chem, 35, p. 4114, DOI: 10.1021/jo00837a619 41 10.1021/jo00837a619 false true Reference 71151516 /api/reference/71151516 42. Gillaizeau-Gauthier 2001: Phosphonate-based bipyridine dyes for stable photovoltaic devices., Inorg Chem, 40, p. 6073, DOI: 10.1021/ic010192e 42 10.1021/ic010192e false true Reference 71151517 /api/reference/71151517 43. Motaleb 2016: An easy and effective method for synthesis and radiolabelling of risedronate as a model for bone imaging., J Label Compd Radiopharm, 59, p. 157, DOI: 10.1002/jlcr.3384 43 10.1002/jlcr.3384 false true Reference 71151518 /api/reference/71151518 44. Gossman 2003: Three hydrates of the bisphosphonate risedronate, consisting of one molecular and two ionic structures., Acta Crystallogr C, 59, p. m33, DOI: 10.1107/S0108270102021996 44 10.1107/S0108270102021996 false true Reference 71151519 /api/reference/71151519 45. Prokhorov 2011: Triazines, tetrazines, and fused ring polyaza systems.Progress in heterocyclic chemistry, p. 403, DOI: 10.1016/B978-0-08-096805-6.00014-0 45 10.1016/B978-0-08-096805-6.00014-0 false true Reference 71151520 /api/reference/71151520 46. Hermer 2015: The new triazine-based porous copper phosphonate [Cu3(PPT)(H2O)3]·10H2O., Dalton Trans, 44, p. 3720, DOI: 10.1039/C4DT03698K 46 10.1039/C4DT03698K false true Reference 71151521 /api/reference/71151521 47. Fu 2015: Two new zinc phosphonates with triazine-based phosphonic acids., Cryst Growth Des, 15, p. 5021, DOI: 10.1021/acs.cgd.5b00983 47 10.1021/acs.cgd.5b00983 false true Reference 71151522 /api/reference/71151522 48. Odobel 2003: Porphyrin dyes for TiO2 sensitization., J Mater Chem, 13, p. 502, DOI: 10.1039/b210674d 48 10.1039/b210674d false true Reference 71151523 /api/reference/71151523 49. Liao 2006: Synthesis of oxygen-containing heterocyclic compounds based on the intramolecular O–H insertion and Wolff rearrangement of a-diazocarbonyl compounds., Tetrahedron Lett, 47, p. 4537, DOI: 10.1016/j.tetlet.2006.05.007 49 10.1016/j.tetlet.2006.05.007 false true Reference 71151524 /api/reference/71151524 50. Sachdeva 2022: Oxygen- and sulphur-containing heterocyclic compounds as potential anticancer agents., Appl Biochem Biotechnol, 194, p. 6438, DOI: 10.1007/s12010-022-04099-w 50 10.1007/s12010-022-04099-w false true Reference 71151525 /api/reference/71151525 51. Sokolov 2024: Phosphorus-containing alkynes in the synthesis of heterocyclic compounds (a review)., Russ J Gen Chem, 94, p. 558, DOI: 10.1134/S1070363224030095 51 10.1134/S1070363224030095 false true Reference 71151526 /api/reference/71151526 52. N’Guyen 2015: Phosphonated furan-functionalized poly(ethyleneoxide)s using orthogonal click chemistries: synthesis and Diels–Alder reactivity., Polym Chem, 6, p. 3024, DOI: 10.1039/C5PY00188A 52 10.1039/C5PY00188A false true Reference 71151527 /api/reference/71151527 53. Matusiak 2013: Phytotoxicity of new furan-derived aminophosphonic acids, N-aryl furaldimines and 5-nitrofuraldimine., J Agric Food Chem, 61, p. 7673, DOI: 10.1021/jf402401z 53 10.1021/jf402401z false true Reference 71151528 /api/reference/71151528 54. Brimble 2022: Pyrans and their benzo derivatives: synthesis.Comprehensive heterocyclic chemistry IV, p. 329 54 false true Reference 71151529 /api/reference/71151529 55. Khandelwal 2020: Use of sustainable organic transformations in the construction of heterocyclic scaffolds.Green approaches in medicinal chemistry for sustainable drug design, p. 245 55 false true Reference 71151530 /api/reference/71151530 56. Pemberton 2019: Heteroaryl phosphonates as noncovalent inhibitors of both serine-and metallocarbapenemases., J Med Chem, 62, p. 8480, DOI: 10.1021/acs.jmedchem.9b00728 56 10.1021/acs.jmedchem.9b00728 false true Reference 71151531 /api/reference/71151531 57. Pathania 2019: Role of sulphur-heterocycles in medicinal chemistry: an update., Eur J Med Chem, 15, p. 486, DOI: 10.1016/j.ejmech.2019.07.043 57 10.1016/j.ejmech.2019.07.043 false true Reference 71151532 /api/reference/71151532 58. Rakitin 2020: Synthesis of sulfur-containing heterocycles by electrophilic addition reactions of disulfur dichloride., Chem Heterocycl Comp, 56, p. 837, DOI: 10.1007/s10593-020-02740-2 58 10.1007/s10593-020-02740-2 false true Reference 71151533 /api/reference/71151533 59. Laxmikeshav 2021: Expedition of sulfur-containing heterocyclic derivatives as cytotoxic agents in medicinal chemistry: a decade update., Med Res Rev, 42, p. 513, DOI: 10.1002/med.21852 59 10.1002/med.21852 false true Reference 71151534 /api/reference/71151534 60. Rabasso 2008: Synthesis of new (3-aminopyrrolidin-3-yl)phosphonic acid- a cucurbitine analogue – and (3-aminotetrahydrothiophen-3-yl)phosphonic acid via phosphite addition to heterocyclic hydrazones., Synthesis, p. 2353 60 false true Reference 71151535 /api/reference/71151535 61. Lamsaf 2019: Molecular and crystal structures and spectroscopic properties of 2-oxo-2-(thiophen-2-yl) ethyl phosphonic acid., J Mol Struct, 1178, p. 73, DOI: 10.1016/j.molstruc.2018.10.015 61 10.1016/j.molstruc.2018.10.015 false true Reference 71151536 /api/reference/71151536 62. Stokes 2003: New phosphonic acid functionalized, regioregular polythiophenes., Macromolecules, 36, p. 7114, DOI: 10.1021/ma034639+ 62 10.1021/ma034639+ false true Reference 71151537 /api/reference/71151537 63. Juaristi 2008: Dioxazines, Oxathiazines, and Dithiazines.Comprehensive heterocyclic chemistry, p. 523 63 false true Reference 71151538 /api/reference/71151538 64. Zhang 2014: Study on a highly selective fluorescent chemosensor for Fe3+ based on 1,3,4-oxadiazole and phosphonic acid., Sens Actuators B Chem, 200, p. 259, DOI: 10.1016/j.snb.2014.04.050 64 10.1016/j.snb.2014.04.050 false true Reference 71151539 /api/reference/71151539 65. Chikkula 2017: Isoxazole–a potent pharmacophore., Int J Pharm Pharm Sci, 9, p. 13, DOI: 10.22159/ijpps.2017.v9i7.19097 65 10.22159/ijpps.2017.v9i7.19097 false true Reference 71151540 /api/reference/71151540 66. Wu 2023: Design, synthesis and bioactivity evaluation of heterocycle-containing mono- and bisphosphonic acid compounds., Molecules, 28, p. 7509, DOI: 10.3390/molecules28227509 66 10.3390/molecules28227509 false true Reference 71151541 /api/reference/71151541 67. Olszewski 2006: Synthesis of thiazole aminophosphine oxides, aminophosphonic and aminophosphinic acids and Cu(II) binding abilities of thiazole aminophosphonic acids., Tetrahedron, 62, p. 2183, DOI: 10.1016/j.tet.2005.12.016 67 10.1016/j.tet.2005.12.016 false true Reference 71151542 /api/reference/71151542 68. Hu 2008: Synthesis of phosphonic acid containing thiadiazole., Heteroat Chem, 19, p. 140, DOI: 10.1002/hc.20395 68 10.1002/hc.20395 false true Reference 71151543 /api/reference/71151543 69. Corinne Dijkmans 2017: Fosfomycin: pharmacological, clinical and future perspectives., Antibiotics, 6, p. 24, DOI: 10.3390/antibiotics6040024 69 10.3390/antibiotics6040024 false true Reference 71151544 /api/reference/71151544 70. Bhattacharyya 2021: Phosphonate functionalized N-heterocyclic carbene Pd(II) complexes as efficient catalysts for Suzuki-Miyaura cross coupling reaction., J Organomet Chem, 953, p. 122067, DOI: 10.1016/j.jorganchem.2021.122067 70 10.1016/j.jorganchem.2021.122067 false true /api/publication/36843128 Chachlaki Elpiniki et al. Synthesis of heterocyclic phosphonic acids. (2026) In: Phosphonate Chemistry, Technology, and Applications pp. 25-46<div class="BookChapter Publication long-list"> <div class="authors"> <img title="Idézőközlemény" style="float: left" src="/frontend/resources/grid/publication-citation-icon.png"> <div class="autype autype0"> <span class="author-name" >Chachlaki Elpiniki </span> ;&nbsp;&nbsp;&nbsp; <span class="author-name" >Demadis Konstantinos D. </span> </div> </div> <div class="title"><a href="/gui2/?mode=browse&params=publication;36843128" target="_blank">Synthesis of heterocyclic phosphonic acids</a></div> <div class="InBook"><div class="chapter-in">In:</div> <div class="authors"> <div class="autype autype-1"> <span class="author-name" >Demadis Konstantinos D. </span> (eds.) </div> </div> <div class="booktitle"><a href="/gui2/?mode=browse&params=publication;36468792" target="_blank">Phosphonate Chemistry, Technology, and Applications : Synthesis, Chemistry, and Biomedical Applications </a></div> <span class="publishedAt">Amszterdam,</span> <span class="publishedAt">London,</span> <span class="publishedAt">Cambridge (MA): <span class="publishers">Elsevier B.V.</span>, <span class="page"> pp 25-46 </span> <span class="year">(2026)</span> </div> <div class="pub-footer"> <span class="language" xmlns="http://www.w3.org/1999/html">Language: English | </span> <span class="identifiers"> <span class="id identifier oa_none" title="none"> <a style="color:blue" title="10.1016/B978-0-443-33374-3.00024-4" target="_blank" href="https://doi.org/10.1016/B978-0-443-33374-3.00024-4"> DOI </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:black" title="105027204208" target="_blank" href="http://www.scopus.com/record/display.url?origin=inward&eid=2-s2.0-105027204208"> Scopus </a> </span> <span class="id identifier oa_none" title="none"> <a style="color:blue" title="https://linkinghub.elsevier.com/retrieve/pii/B9780443333743000244" target="_blank" href="https://linkinghub.elsevier.com/retrieve/pii/B9780443333743000244"> Other URL </a> </span> </span> <span class="bookchapter-ids">Book link(s):</span> <span class="identifiers"> <span class="id identifier oa_none" title="none"> <a style="color:black" title="10.1016/C2024-0-00017-3" target="_blank" href="https://doi.org/10.1016/C2024-0-00017-3"> DOI </a> </span> <span class="id identifier oa_none" title="none"> <span class="isbnOrIssn"> ISBN: </span> <a style="color:black" title="9780443333743" target="_blank" href="https://www.worldcat.org/search?q=isbn%3A9780443333743"> 9780443333743 </a> </span> </span> <div class="publication-citation"> <a target="_blank" href="/api/publication?cond=citations.related;eq;36843128&sort=publishedYear,desc&sort=title"> Number of cited publications: 2 </a> </div> <div class="mtid"><span class="long-pub-mtid">Publication: 36843128</span> | <span class="status-data status-APPROVED"> Published </span> <span class="long-book-mtid">Book: 36468792</span> Citing | <span class="type-subtype">Chapter in Book ( Chapter ) </span> | <span class="pub-category">Scientific</span> | <span class="publication-sourceOfData">DOI XML</span> </div> <div class="lastModified">Last Modified: 2026.03.03. 14:59 Katalin Andódy (BME admin4) </div> </div> </div>