Abstract
Dialkyl 1-alkyl(aryl)-2-nitroeth-1-enylphosphonates were prepared by treatment of dialkyl 1-alkyl(aryl)-1-hydroxyl-2-nitroalkylphosphonates with thionyl chloride and pyridine. The dehydration process underwent stereospecifically providing exclusively the E-isomers. An E2 reaction mechanism was suggested.
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