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Phosphorus, Sulfur, and Silicon and the Related Elements Volume 184, 2009 - Issue 4: Honoring the 70th Birthday of Marian Mikolajczyk
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Original Articles

Synthesis of Phosphonic Acids Possessing Isoindolin-1-one Moiety: Unexpected Acid-Catalyzed C-P-Bond Cleavage

Georgiy O. Kachkovskyi Institute of Bioorganic Chemistry and Petrochemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine
&
Oleg I. Kolodiazhnyi Institute of Bioorganic Chemistry and Petrochemistry of the National Academy of Sciences of Ukraine, Kyiv, Ukraine
Pages 890-907 | Received 21 Dec 2007, Accepted 24 Jan 2008, Published online: 26 Mar 2009

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A. Mejri, L. Mansour & N. Hamdi. (2022) Synthesis and Antimicrobial Activity of Some of Isoindolin-1-One-3-Phosphonates under Mild and Solvent-Free Conditions. Polycyclic Aromatic Compounds 0:0, pages 1-10.
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OlegI. Kolodiazhnyi, EvgenV. Gryshkun, AnastasyaO. Kolodiazhna, GeorgyO. Kachkovskyi, OlgaO. Kolodiazhna, SergyiYu. Sheiko & ViacheslavN. Zemlianoi. (2011) New Methods for the Synthesis of Phosphonic Analogues of Natural Compounds. Phosphorus, Sulfur, and Silicon and the Related Elements 186:4, pages 644-651.
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GeorgiyO. Kachkovskyi, LudmylaA. Kononets, VsevolodYu. Tanchuk, AndriyI. Vovk & OlegI. Kolodiazhnyi. (2011) Synthesis and Evaluation of 1-Aryl-1-(7-carboxy-isoindolin-1-one-2-yl)methylphosphonic Acid Derivatives as Inhibitors of Protein Tyrosine Phosphatase. Phosphorus, Sulfur, and Silicon and the Related Elements 186:4, pages 956-957.
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GeorgiyO. Kachkovskyi & OlegI. Kolodiazhnyi. (2010) Synthesis of the Phosphonoanalogue of Benzo[c]pyroglutamic Acid. Phosphorus, Sulfur, and Silicon and the Related Elements 185:12, pages 2441-2448.
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GeorgiyO. Kachkovskyi & OlegI. Kolodiazhnyi. (2010) Synthesis of Phosphonoindoprofen. Phosphorus, Sulfur, and Silicon and the Related Elements 185:11, pages 2238-2242.
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Articles from other publishers (24)

Hamida Jelali, Ibrahim S. Al Nasr, Waleed S. Koko, Tariq A. Khan, Eric Deniau, Mathieu Sauthier, Faisal Alresheedi & Naceur Hamdi. (2022) Synthesis, characterization and in vitro bioactivity studies of isoindolin‐1‐3‐phosophonate compounds. Journal of Heterocyclic Chemistry 59:3, pages 493-506.
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Ádám Tajti, Nóra Tóth, Bettina Rávai, István Csontos, Pál Tamás Szabó & Erika Bálint. (2020) Study on the Microwave-Assisted Batch and Continuous Flow Synthesis of N-Alkyl-Isoindolin-1-One-3-Phosphonates by a Special Kabachnik–Fields Condensation. Molecules 25:14, pages 3307.
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Piotr M. Zagórski, Andrzej Jóźwiak, Mieczysław W. Płotka & Dariusz Cal. (2016) A hitherto undescribed addition of the lithium salt of dimethyl methylphosphonate to N-substituted phthalimides. Tetrahedron Letters 57:17, pages 1835-1837.
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Mehdi Adib, Ehsan Sheikhi, Rozita Yazzaf, Hamid Reza Bijanzadeh & Peiman Mirzaei. (2016) An efficient, three-component synthesis of isoindolin-1-one-3-phosphonates under mild and solvent-free conditions. Tetrahedron Letters 57:8, pages 841-844.
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Mario Ordóñez, José Luis Viveros-Ceballos, Carlos Cativiela & Francisco J. Sayago. (2015) An update on the stereoselective synthesis of α-aminophosphonic acids and derivatives. Tetrahedron 71:12, pages 1745-1784.
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Nagendra Prasad Muddala, Baskar Nammalwar & Richard A. Bunce. (2015) Expeditious synthesis of (±)-diethyl 2-alkyl- and 2-aryl-(3-oxoisoindolin-1-yl)phosphonates catalysed by OSU-6. RSC Advances 5:36, pages 28389-28393.
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Andrzej Jóźwiak, Piotr M. Zagórski, Mieczysław W. Płotka & Dariusz Cal. (2014) Synthesis of phosphorylated isoindolinone derivatives. Tetrahedron Letters 55:15, pages 2420-2422.
Crossref
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 936 936 .
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 86 86 .
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 489 489 .
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 440 440 .
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 2390 2390 .
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 2154 2154 .
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 2153 2153 .
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 1918 1918 .
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 1917 1917 .
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 1678 1678 .
M. Kumar. 2014. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 1677 1677 .
M. Kumar. 2013. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 3743 3743 .
M. Kumar. 2013. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 3717 3717 .
M. Kumar. 2013. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 3706 3706 .
M. Kumar. 2013. Chemical Shifts and Coupling Constants for Phosphorus-31. Chemical Shifts and Coupling Constants for Phosphorus-31 3305 3305 .
Fedor I. Zubkov, Inga K. Airiyan, Julya D. Ershova, Timur R. Galeev, Vladimir P. Zaytsev, Eugeniya V. Nikitina & Alexey V. Varlamov. (2012) Aromatization of IMDAF adducts in aqueous alkaline media. RSC Advances 2:10, pages 4103.
Crossref
José Luis Viveros-Ceballos, Carlos Cativiela & Mario Ordóñez. (2011) One-pot three-component highly diastereoselective synthesis of isoindolin-1-one-3-phosphonates under solvent and catalyst free-conditions. Tetrahedron: Asymmetry 22:13, pages 1479-1484.
Crossref

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