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<p>can also be viewed as di-esters of phosphonic acid: (O=PH(OR)<sub>2</sub>) undergo a palladium-catalyzed coupling reaction with an <a href="page.php?w=aryl_halide">aryl halide</a> to form a phosphonate.</p>

<p><big>Michaelis-Arbuzov reaction</big></p>
<p>Phosphonic esters are prepared using the <a href="page.php?w=Michaelis-Arbuzov_reaction">Michaelis-Arbuzov reaction</a>. For example, methyl iodide catalyses the conversion of trimethylphosphite to the phosphonate ester <a href="page.php?w=dimethyl_methylphosphonate">dimethyl methylphosphonate</a>:<br/>
:P(OMe)<sub>3</sub></p><p>
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