Silver bromate

<h2 id="uses">Uses</h2>
<p>Silver bromate can be used as an <a href="/facts/Oxidant/1FQzB8pQ">oxidant</a> for the transformation of <a href="/facts/Tetrahydropyranyl/kQ3m5lfg">tetrahydropyranyl</a> <a href="/facts/Ether/jwDg0IKr">ethers</a> to <a href="/facts/Carbonyl_compound/KJ71bo3X">carbonyl compounds</a>.<a class="footnote-ref" id="fnref:2" href="#fn:2"><sup>2</sup></a>
</p>

<h2 id="external-links">External links</h2>
<ul><li><a href="http://pubs.acs.org/doi/abs/10.1021/j100300a047">Silver bromate solubility</a></li>
<li><a href="http://www.chemthes.com/entity_datapage.php?id=1418">Chemical data</a></li></ul>

<h2 id="references">References</h2>

<ol>
<li id="fn:1"><p>Perry, Dale L. (2011). Handbook of inorganic compounds (2nd ed.). Boca Raton: Taylor & Francis. p. 365. ISBN 978-1-4398-1461-1. OCLC 587104373. <a href="978-1-4398-1461-1" target="_blank">978-1-4398-1461-1</a> <a href="#fnref:1" class="footnote-back-ref">↩</a></p></li>
<li id="fn:2"><p>Mohammadpoor-Baltork, Iraj; Nourozi, Ali Reza (1999). "Efficient and Selective Oxidative Deprotection of Tetrahydropyranyl Ethers, Ethylene Acetals and Ketals with Silver and Sodium Bromates in the Presence of Aluminum Chloride". Synthesis. 1999 (3): 487–490. doi:10.1055/s-1999-3410. S2CID 196725503. <a href="/wiki/Doi_(identifier)" target="_blank">/wiki/Doi_(identifier)</a> <a href="#fnref:2" class="footnote-back-ref">↩</a></p></li>
</ol>

Silver bromate open-in-new

Silver bromate