<?xml version="1.0" encoding="UTF-8"?><xml><records><record><source-app name="Biblio" version="7.x">Drupal-Biblio</source-app><ref-type>17</ref-type><contributors><authors><author><style face="normal" font="default" size="100%">Specklin, Simon</style></author><author><style face="normal" font="default" size="100%">Gallier, Florian</style></author><author><style face="normal" font="default" size="100%">Mezaache, Roufia</style></author><author><style face="normal" font="default" size="100%">Hassina Harkat</style></author><author><style face="normal" font="default" size="100%">Yénimégué, Albert</style></author><author><style face="normal" font="default" size="100%">Jean-Marc Weibel</style></author><author><style face="normal" font="default" size="100%">Aurélien Blanc</style></author><author><style face="normal" font="default" size="100%">Patrick Pale</style></author></authors></contributors><titles><title><style face="normal" font="default" size="100%">Copper(II) Bromide as Efficient Catalyst for Silyl- to Bisarylmethyl Ethers Interconversion (Transprotection)</style></title><secondary-title><style face="normal" font="default" size="100%">Tetrahedron Letters</style></secondary-title></titles><dates><year><style  face="normal" font="default" size="100%">2011</style></year><pub-dates><date><style  face="normal" font="default" size="100%">09</style></date></pub-dates></dates><urls><web-urls><url><style face="normal" font="default" size="100%">https://www.sciencedirect.com/science/article/abs/pii/S0040403911014754?via%3Dihub</style></url></web-urls></urls><volume><style face="normal" font="default" size="100%">52</style></volume><pages><style face="normal" font="default" size="100%">5820-5823</style></pages><language><style face="normal" font="default" size="100%">eng</style></language><abstract><style face="normal" font="default" size="100%">&lt;p id=&quot;sp010&quot; style=&quot;text-align: justify;&quot;&gt;
	Primary and secondary silylated alcohols are easily converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr&lt;sub&gt;2&lt;/sub&gt;&amp;nbsp;as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
&lt;/p&gt;

&lt;h2 style=&quot;text-align: justify;&quot;&gt;
	Graphical abstract
&lt;/h2&gt;

&lt;p id=&quot;sp005&quot; style=&quot;text-align: justify;&quot;&gt;
	Primary and secondary silylated alcohols are easily and rapidly converted to bis(methoxyphenyl)methyl (BMPM) ethers in good yields using CuBr&lt;sub&gt;2&lt;/sub&gt;&amp;nbsp;as catalyst in acetonitrile at room temperature. Various other protecting groups are compatible with this mild and convenient process.
&lt;/p&gt;

&lt;figure id=&quot;f0025&quot;&gt;
	&lt;p style=&quot;text-align: justify;&quot;&gt;
		&lt;img alt=&quot;&quot; height=&quot;107&quot; src=&quot;https://ars.els-cdn.com/content/image/1-s2.0-S0040403911014754-fx1.jpg&quot;&gt;
	&lt;/p&gt;
&lt;/figure&gt;
</style></abstract><issue><style face="normal" font="default" size="100%">44</style></issue></record></records></xml>