Pure and Applied Chemistry

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• Ballester Jorge, Gatignol Jérémie, Schmidt Guntram, Alayrac Carole, Gaumont Annie-Claude, Taillefer Marc: A Copper-Catalyzed Variant of the Michaelis-Arbuzov Reaction. ChemCatChem 2014, n/a. <http://dx.doi.org/10.1002/cctc.201301029>
• Brewster Richard, Vandergeten Marie-Christine, Montel Florian: Syntheses of Heteraphosphacyclanes: Follow the Guide!. Eur. J. Org. Chem. 2014, 2014, 905. <http://dx.doi.org/10.1002/ejoc.201301299>
• GOLLA MADHAVA, SYED RASHEED, KATLA VENKATA RAMANA, DEVINENI SUBBA RAO, KONDAPALLI NARESH, CHAMARTHI NAGA RAJU: LaCl3.7H2O: An efficient catalyst for the synthesis of phosphinates (Michaelis–Arbuzov reaction) under neat conditions and their potential antimicrobial activity. J Chem Sci 2014. <http://dx.doi.org/10.1007/s12039-013-0550-3>
• Ng Yong Xiang, Mathey Francois: Using Monovalent Phosphorus Compounds to Form P-C Bonds. Angew. Chem. 2013, 125, 14390. <http://dx.doi.org/10.1002/ange.201306643>
• Ng Yong Xiang, Mathey Francois: Using Monovalent Phosphorus Compounds to Form P-C Bonds. Angew. Chem. Int. Ed. 2013, 52, 14140. <http://dx.doi.org/10.1002/anie.201306643>
• van Kalkeren Henri A., van Delft Floris L., Rutjes Floris P. J. T.: Organophosphorus Catalysis to Bypass Phosphine Oxide Waste. ChemSusChem 2013, 6, 1615. <http://dx.doi.org/10.1002/cssc.201300368>
• THORAT PRASHANT B, GOSWAMI SANTOSH V, MAGAR RUPALI L, BHUSARE SUDHAKAR R: Organocatalysis for the synthesis of optically active β-malonophosphonates. J Chem Sci 2013, 125, 1109. <http://dx.doi.org/10.1007/s12039-013-0487-6>
• Ho Mei-Chan, Chao Ching-Hsun, Lo An-Ya, Chen Chun-Hua, Wu Ren-Jye, Tsai Mei-Hui, Huang Yi-Chia, Whang Wha-Tzong: Significant improvement in the thermoelectric properties of zwitterionic polysquaraine composite films. Materials Chemistry and Physics 2013, 141, 920. <http://dx.doi.org/10.1016/j.matchemphys.2013.06.024>
• Chinthaparthi Radha Rani, Gangireddy Chandra Sekhar Reddy, Mudumala Veeranarayana Reddy, Gundluru Mohan, Chamarthi Nagaraju, Cirandur Suresh Reddy: CeCl3·7H2O: a highly efficient catalyst for the synthesis of 1-substituted-octahydro-[1,3,2]diazaphospholo[1,5-a]pyridine-1-oxide. Tetrahedron Letters 2013, 54, 6071. <http://dx.doi.org/10.1016/j.tetlet.2013.08.115>
• Dhokale Ranjeet A., Mhaske Santosh B.: P-Arylation: Arynes to Aryl-Phosphonates, -Phosphinates, and -Phosphine Oxides. Org. Lett. 2013, 15, 2218. <http://dx.doi.org/10.1021/ol400780f>
• Giffin Kaitie A., Harrison Daniel J., Korobkov Ilia, Baker R. Tom: Activation of C–F and Ni–C Bonds of [P,S]-Ligated Nickel Perfluorometallacycles. Organometallics 2013, 32, 7424. <http://dx.doi.org/10.1021/om400933k>
• Hussain Hidayat, Green Ivan R., Krohn Karsten, Ahmed Ishtiaq: Advances in the total synthesis of biologically important callipeltosides: a review. Nat. Prod. Rep. 2013, 30, 640. <http://dx.doi.org/10.1039/c3np20110d>
• Jiao Yunzhe, Brennessel William W., Jones William D.: A tris(pyrazolyl)borate rhodium phosphite complex that undergoes an Arbusov-like rearrangement. Acta Crystallogr C Cryst Struct Commun 2013, 69, 939. <http://dx.doi.org/10.1107/S0108270113015953>
• Ni Shengjun, Ma Shengming, Chen Jie: Tuning of Regioselectivity in Inorganic Iodide-Catalyzed Alkylation of 2-Methoxyfurans via Electronic and Steric Effects. Synth Catal 2012, 354, 1114. <http://dx.doi.org/10.1002/adsc.201100337>
• Li Xiubin, Hu Gaobo, Luo Ping, Tang Guo, Gao Yuxing, Xu Pengxiang, Zhao Yufen: Palladium(II)-Catalyzed Hydration of Alkynylphosphonates to β-Ketophosphonates. Adv. Synth. Catal. 2012, 354, 2427. <http://dx.doi.org/10.1002/adsc.201200420>
• Jambal Irekhjargal, Kefurt Karel, Hlaváčková Martina, Moravcová Jitka: Synthesis of 2-fluoro and 4-fluoro galactopyranosyl phosphonate analogues of UDP-Gal. Carbohydrate Research 2012, 360, 31. <http://dx.doi.org/10.1016/j.carres.2012.07.015>
• Davis Matthew C., Groshens Thomas J.: Dimerization of resveratrol trimethyl ether by phosphotungstic acid, structure confirmation of resformicol A and B. Tetrahedron Letters 2012, 53, 3521. <http://dx.doi.org/10.1016/j.tetlet.2012.04.132>
• Ho Mei-Chan, Chao Ching-Hsun, Chen Chun-Hua, Wu Ren-Jye, Whang Wha-Tzong: Effect of Ionic Liquid on Structure and Properties of Polysquaraines. Macro­molecules 2012, 45, 3010. <http://dx.doi.org/10.1021/ma202526z>
• Arkhypchuk Anna I., Santoni Marie-Pierre, Ott Sascha: Revisiting the Phospha-Wittig–Horner Reaction. Organomettalics 2012, 31, 1118. <http://dx.doi.org/10.1021/om201158k>
• van Kalkeren Henri A., van Delft Floris L., Rutjes Floris P. J. T.: Catalytic Appel reactions. Pure Appl. Chem. 2012, 1. <http://dx.doi.org/10.1351/PAC-CON-12-06-13>
• Wei Wei, Ji Jian-Xin: Catalytic and Direct Oxyphosphorylation of Alkenes with Dioxygen and H-Phosphonates Leading to β-Ketophosphonates. angew chemie 2011, 123, 9263. <http://dx.doi.org/10.1002/ange.201100219>
• Wei Wei, Ji Jian-Xin: Catalytic and Direct Oxyphosphorylation of Alkenes with Dioxygen and H-Phosphonates Leading to β-Ketophosphonates. Angew Chem Int E 2011, 50, 9097. <http://dx.doi.org/10.1002/anie.201100219>
• Doğan Özdemir, Babiz Hakan, Gözen Ayşe Gül, Budak Songül: Synthesis of 2-aziridinyl phosphonates by modified Gabriel–Cromwell reaction and their antibacterial activities. Eur Med Chem 2011, 46, 2485. <http://dx.doi.org/10.1016/j.ejmech.2011.03.037>
• Xu Qing, Han Li-Biao: Metal-catalyzed additions of H–P(O) bonds to carbon–carbon unsaturated bonds. J Organomet Chem 2011, 696, 130. <http://dx.doi.org/10.1016/j.jorganchem.2010.08.043>
• Lichtenthaler Frieder W.: 2-Oxoglycosyl (“Ulosyl”) and 2-Oximinoglycosyl Bromides: Versatile Donors for the Expedient Assembly of Oligosaccharides with β-d-Mannose, β-l-Rhamnose, N-Acetyl-β-d-mannosamine, and N-Acetyl-β-d-mannosaminuronic Acid Units. Chemistry Review 2011, 111, 5569. <http://dx.doi.org/10.1021/cr100444b>
• Aluri Bhaskar Reddy, Niaz Basit, Kindermann Markus K., Jones Peter G., Heinicke Joachim: PC–N-Heterocycles: synthesis of biaryl-type 1,3-benzazaphospholes with ortho-substituted phenyl or 2-heteroaryl groups. Dalton Trans 2011, 40, 211. <http://dx.doi.org/10.1039/c0dt00881h>
• Brunner H., Zettlmeier W.: Synthese Chiraler Phosphinoxide Und Phosphine Durch Michaelis-Arbuzov-Umlagerung. Bull Soc Chim Belges 2010, 100, 247. <http://dx.doi.org/10.1002/bscb.19911000310>
• Yavari Issa, Mirzaei Anvar, Khalili Gholamhossein: Solvent-Free Synthesis of Diphenyl [2-(Aminocarbonyl)-1,2-dihydroisoquinolin-1-yl]phosphonates from Isoquinoline, Isocyanates, and Diphenyl Phosphonate. HCA 2010, 93, 654. <http://dx.doi.org/10.1002/hlca.200900247>
• Castelijns Marianne M. C. F., van Aken Dirk, Schipper Pieter, van Lier Johan J. C., Buck Henk M.: Salt-induced conversions of P(V) into P(IV) in solvents of different polarity. A tentative model for the initiation of conformational changes in DNA via the P(IV) residues. Recl Trav Chim Pays-Bas 2010, 99, 380. <http://dx.doi.org/10.1002/recl.19800991203>
• Broekhof N. L. J. M., van Elburg P., van der Gen A.: The synthesis of α-amino-substituted diphenylphosphine oxides. Recl Trav Chim Pays-Bas 2010, 103, 312. <http://dx.doi.org/10.1002/recl.19841031103>
• de Vroom E., Spierenburg M. L., Dreef C. E., van der Marel G. A., van Boom J. H.: A general procedure to convert H-phosphonate mono- or diesters of nucleic acids into valuable phosphate di- or triesters. Recl Trav Chim Pays-Bas 2010, 106, 65. <http://dx.doi.org/10.1002/recl.19871060206>
• de Vroom E., Dreef C. E., van den Elst H., van der Marel G. A., van Boom J. H.: Preparation of internucleotide phosphate analogues via the corresponding H-phosphonate diester. Recl Trav Chim Pays-Bas 2010, 107, 592. <http://dx.doi.org/10.1002/recl.19881071004>
• Hilgetag Günter, Teichmann Herbert: Organische Derivate von Säuren des Phosphors. Z Chem 2010, 11, 1. <http://dx.doi.org/10.1002/zfch.19710110102>
• Groß Hans, Costisella Burkhard: Synthesen und Einsatzmöglichkeiten von organischen Phosphor- und Phosphonsäurederivaten. Z Chem 2010, 17, 281. <http://dx.doi.org/10.1002/zfch.19770170802>
• Scaravelli Federico, Bacchi Sergio, Massari Luca, Curcuruto Ornella, Westerduin Pieter, Maton William: Efficient method to prepare diethylphosphonacetamides. Tetrahetron Lett 2010, 51, 5154. <http://dx.doi.org/10.1016/j.tetlet.2010.07.125>
• Dabkowski Wojciech, Ozarek Alfred, Olejniczak Sebastian, Cypryk Marek, Chojnowski Julian, Michalski Jan: Studies on the Efficient Generation of PhosphorusCarbon Bonds via a Rearrangement of P^III Esters Catalysed by Trimethylhalosilanes. Chem Eur J 2009, 15, 1747. <http://dx.doi.org/10.1002/chem.200800435>
• Sobhani Sara, Vafaee Asieh: Efficient one-pot synthesis of β-hydroxyphosphonates: regioselective nucleophilic ring opening reaction of epoxides with triethyl phosphite catalyzed by Al(OTf)3. Tetrahedron 2009, 65, 7691. <http://dx.doi.org/10.1016/j.tet.2009.06.106>
• Tharmaraj P., Kodimunthiri D., Sheela C.D., Prakash P.: Bis -(3,5-dimethyl-pyrazolyl-1-methyl)-(3-phosphanyl-propyl)-amine complexes of copper(II), nickel(II), and cobalt(II). J Coord Chem 2009, 62, 1347. <http://dx.doi.org/10.1080/00958970802546032>
• Tharmaraj P., Kodimunthiri D., Prakash P., Sheela C.D.: Catalytic and biological activity of transition metal complexes of salicylaldiminopropylphosphine. J Coord Chem 2009, 62, 2883. <http://dx.doi.org/10.1080/00958970902934740>
• Durst H. D., Rohrbaugh D. K., Munavalli S.: Stereoselective Synthesis of Phosphoryl Derivatives. Phosphorus Sulfur Silicon Relat Elem 2009, 184, 2902. <http://dx.doi.org/10.1080/10426500802591655>
• Synthesis of Chiral C₂-symmetric Palladium and Rhodium SCS Pincers. Bulletin of the Korean Chemical Society 2009, 30, 23. <http://dx.doi.org/10.5012/bkcs.2009.30.1.023>
• One Pot Synthesis of Variously Substituted &#x03B3;-Ketophosphonates Using Pentacovalent Oxaphospholenes. Bulletin of the Korean Chemical Society 2009, 30, 239. <http://dx.doi.org/10.5012/bkcs.2009.30.1.239>
• Lyubimtsev Alexey, Misir Miraç N., Calvete Mario, Hanack Michael: Titanium Phthalocyanines with Axial Phenylenevinylenes. Eur J Org Chem 2008, 2008, 3209. <http://dx.doi.org/10.1002/ejoc.200701197>
• Kumamoto Hiroki, Topalis Dimitri, Broggi Julie, Pradère Ugo, Roy Vincent, Berteina-Raboin Sabine, Nolan Steven P., Deville-Bonne Dominique, Andrei Graciela, Snoeck Robert, Garin Daniel, Crance Jean-Marc, Agrofoglio Luigi A.: Preparation of acyclo nucleoside phosphonate analogues based on cross-metathesis. Tetrahedron 2008, 64, 3517. <http://dx.doi.org/10.1016/j.tet.2008.01.140>
• Evans David A., Burch Jason D., Hu Essa, Jaeschke Georg: Enantioselective total synthesis of callipeltoside A: two approaches to the macrolactone fragment. Tetrahedron 2008, 64, 4671. <http://dx.doi.org/10.1016/j.tet.2008.02.001>
• Hosseini-Sarvari Mona, Etemad Samane: Nanosized zinc oxide as a catalyst for the rapid and green synthesis of β-phosphono malonates. Tetrahedron 2008, 64, 5519. <http://dx.doi.org/10.1016/j.tet.2008.03.095>
• Delain-Bioton Lise, Villemin Didier, Jaffrès Paul-Alain: ω-Alkyne-Mono- and Diphosphonates – Synthesis and Sonogashira Cross-Coupling Reaction with Aryl Halides. Eur J Org Chem 2007, 2007, 1274. <http://dx.doi.org/10.1002/ejoc.200600556>
• Liu Yi, Zhang Xiyun, Klivansky Liana M., Koshkakaryan Gayane: Enhancing the reactivity of 1,2,3-triazoles in “click” macrocycles by face-to-face dibenzylammonium ion binding. Chem Commun 2007, 4773. <http://dx.doi.org/10.1039/b711505a>
• Sardarian A. R., Shahsavari‐Fard Z.: Convenient and Regioselective One‐Pot Solvent‐Free Synthesis of ß‐Hydroxyphosphonates. Synth Comm 2007, 37, 289. <http://dx.doi.org/10.1080/00397910601033757>
• Rill Christoph, Ivanovici Sorin, Kickelbick Guido: Hybrid Nanoparticles Prepared by In-situ and Post-synthetic Surface Modification of Lanthanide-Based Nanoparticles with Phosphonic Acid Derivatives. Mat Res Symp Proc 2007, 1007, 1007-S12-02. <http://dx.doi.org/10.1557/PROC-1007-S12-02>
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• Nathaniel Rachel, Mineva Tzonka, Nikolova Rositca, Bojilova Anka: Density functional study of the interaction of 3-(ω-bromoacetyl)coumarin with phosphites. Int J Quantum Chem 2006, 106, 1357. <http://dx.doi.org/10.1002/qua.20893>
• Tarnowski Andrej, Retz Oliver, Bär Thomas, Schmidt Richard R.: Synthesis of Sphingosine-1-phosphonate and Homosphingosine-1-phosphonate. Eur J Org Chem 2005, 2005, 1129. <http://dx.doi.org/10.1002/ejoc.200400671>
• Mlostoń Grzegorz, Majchrzak Agnieszka, Rutkowska Marzena, Woznicka Marta, Linden Anthony, Heimgartner Heinz: Synthesis and Reactions of a New Cyclobutanethione Derivative. HCA 2005, 88, 2624. <http://dx.doi.org/10.1002/hlca.200590203>
• Ordóñez Mario, Hernández-Fernández Eugenio, Xahuentitla Janet, Cativiela Carlos: Asymmetric alkylation of dimethoxyphosphoryl-N-[1-(S)-α-methylbenzyl]acetamide enolates. Synthesis of both stereoisomers from the same source of chirality by changing the equivalents of LDA. Chem Commun 2005, 1336. <http://dx.doi.org/10.1039/b416616g>
• The Development of a New Synthetic Method for Cyclic Dehydroamino Acid Derivatives by the Intramolecular Cyclization Reaction via Imine Anion. Journal of the Korean Chemical Society 2005, 49, 56. <http://dx.doi.org/10.5012/jkcs.2005.49.1.056>
• Kim Bong Soo, Joo Sung-Hoon, Oh Dongkeun, Cha Soon Wook, Choi Don Soo, Lee Cheol Eui, Jin Jung-Il: Charge mobilities and luminescence characteristics of blue-light emitting bent carbazole trimers connected through vinylene linkers—effect of nitrile substituents. Synthetic Metal 2004, 145, 229. <http://dx.doi.org/10.1016/j.synthmet.2004.05.010>
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