RAPID AND EFFICIENT ARBUZOV REACTION UNDER MICROWAVE IRRADIATION
- 1 January 1998
- journal article
- research article
- Published by Taylor & Francis in Phosphorus, Sulfur, and Silicon and the Related Elements
- Vol. 133 (1) , 209-213
- https://doi.org/10.1080/10426509808032465
Abstract
Diethyl alkylphosphonates are efficiently and rapidly prepared in good yields (75–99%) from trialkylphosphates and alkyl halides under short microwaves irradiations.Keywords
This publication has 13 references indexed in Scilit:
- Microwave assisted organic reactionsTetrahedron, 1995
- Synthesis of Quinoxalines Under Focussed Microwave IrradiationSynthetic Communications, 1995
- Dry Synthesis Under Microwave Irradiation: A rapid and efficient coupling of naphtholsSynlett, 1994
- Synthesis of layered Zr(O3PCH2CH2COCl)2 from Zr(O3PCH2CH2COOH)2Chemistry of Materials, 1991
- Polyether derivatives of zirconium phosphateInorganic Chemistry, 1985
- Cyclopentenones from β, ∊-Diketo Phosphonates. Synthesis of cis -JasmoneSynthetic Communications, 1975
- Isolation of cis and trans Isomers of Some Oxaphosphorinans.Acta Chemica Scandinavica, 1967
- Nitrogen Mustard Derivatives Containing the Phosphonate Group1Journal of the American Chemical Society, 1959
- Mechanism of the Michaelis-Arbuzov Reaction: Olefin FormationThe Journal of Organic Chemistry, 1959
- Bond Refractions and the Nature of Phosphorus-Oxygen BondsJournal of the American Chemical Society, 1958