Polyethylene Glycol–Promoted Dialkyl, Aryl/Heteroaryl Phosphonates

REFERENCES

• Sikorski , J. A. ; Logusch , E. W. Aliphatic carbon–phosphorus compounds as herbicides ; In Hand book of Organophosphorus Chemistry ; R. Engel , (Ed.); Marcel Dekker : New York , 1992 .
   Google Scholar
• Eto , M. Phosphorus-containing insecticides ; In Handbook of Organophosphorus Chemistry ; R. Engel , (Ed.); Marcel Dekker : New York , 1992 .
   Google Scholar
• Saady , M. ; Lebeau , L. ; Mioskowski , C. Synthesis of di- and triphosphate ester analogs via a modified Michaelis–Arbuzov reaction . Tetrahedron Lett. 1995 , 36 , 5183 – 5186 .
   Web of Science ®Google Scholar
• (a) Yadav , V. K. A practical approach to homo trialkyl phosphonates: A catalytic Michaelis–Arbuzov reaction . Synth. Commun. 1990 , 20 , 239 – 246 ; (b) Brunner , H. ; Zettlmeier , W. Synthese chiraler Phosphinoxide und Phosphine durch Michaelis-Arbuzov-Umlagerung . Bull. Soc. Chim. Belg. 1991 , 100 , 247 .
   Web of Science ®Google Scholar
• (a) Rose , U. 2-Aryl-substituted 4H-3,1-benzoxazin-4-ones as novel active substances for the cardiovascular system . J. Heterocycl. Chem. 1991 , 28 , 2005 – 2012 ; (b) Toshima , K. ; Yamagushi , H. ; Jyojima , T. ; Nogushi , Y. ; Nakata , M. ; Matsumura , S. Total synthesis of bafilomycin A1, 2: The assemblage and completion of the synthesis . Tetrahedron Lett. 1996 , 37 , 1073 – 1076 .
   Web of Science ®Google Scholar
• Renard , P. Y. ; Varon , P. ; Mioskowski , C. Trimethylsilyl halide-promoted Michaelis–Arbuzov rearrangement . Org. Lett. 2003 , 5 , 1661 – 1664 .
   PubMed Web of Science ®Google Scholar
• Renard , P. Y. ; Varon , P. ; Leclerc , E. ; Valleix , A. ; Mioskowski , C. Lewis acid–catalyzed roomtemperature Michaelis–Arbuzov rearrangement . Angew. Chem. Int. Ed. 2003 , 42 , 2389 – 2392 .
   PubMed Web of Science ®Google Scholar
• Mataveeva , E. V. ; Odinets , I. L. ; Kozlov , V. A. ; Shaplov , A. S. ; Mastryukova , T. A. Ionic liquid–promoted Michaelis–Arbuzov rearrangement . Tetrahedron Lett. 2006 , 47 , 7645 .
   Web of Science ®Google Scholar
• (a) Vasudevan , V. N. ; Rajender , S. V. Microwave-accelerated Suzuki cross-coupling reaction in polyethylene glycol (PEG) . Green Chem. 2001 , 3 , 146 – 148 ; (b) Haimov , A. ; Neumann , R. Polyethylene glycol as a nonionic liquid solvent for polyoxometalate–catalyzed aerobic oxidation . Chem. Commun. 2002 , 876 – 877 ; (c) Heiss , L. ; Gais , H. J. Polyethylene glycol monomethyl ether–modified pig liver esterase: Preparation, characterization, and catalysis of enantioselective hydrolysis in water and acylation in organic solvents . Tetrahedron Lett. 1995 , 36 , 3833 – 3836 ; (d) Chandrasekar , S. ; Narasihmulu , C. ; Shameem , S. S. ; Reddy , N. R. Osmium tetroxide in poly(ethylene glycol)(PEG): A recyclable reaction medium for rapid asymmetric dihydroxylation under Sharpless conditions . Chem. Commun. 2003 , 1716 – 1717 ; (e) Tanemura , K. ; Suzuki , T. ; Nishida , Y. ; Horaguchi , T. Aldol condensation in water using polyethylene glycol 400 . Chem. Lett. 2005 , 34 , 576 ; (f) Kamal , A. ; Reddy , D. R. ; Rajendar . Polyethylene glycol (PEG) as an efficient recyclable medium for the synthesis of β-amino sulfides . Tetrahedron Lett. 2006 , 47 , 2261 – 2264 .
   Web of Science ®Google Scholar
• Veera Narayana Reddy , M. ; Kishore Kumar Reddy , K. ; Bhupendra Reddy , C. ; Siva Kumar , B. ; Suresh Reddy , C. ; Devendranath Reddy , C. Synthesis and antimicrobial activity of bisphosphonates. J. Chem. Res. 2009, 4, 258–260.
   Web of Science ®Google Scholar
• Syam Prasad , G. ; Manjunath , M. ; Kishore Kumar Reddy , K. ; Vijaya Sarathi Reddy , O. ; Suresh Reddy , C. Synthesis and antibacterial activity of new aryl/alkyl phosphonates via Michaelis–Arbuzov Rearrangement . Arkivoc 2006 , 16 , 128 – 135 .
   Google Scholar
• Armarego , W. L.F. ; Perrin , D. D. Purification of Laboratory Chemicals, ; , 4th ed. Butterworth, Heinemann : Oxford , UK, 1997 .
   Google Scholar