<?xml version="1.0" encoding="UTF-8" standalone="yes"?><oembed><version><![CDATA[1.0]]></version><provider_name><![CDATA[amphoteros]]></provider_name><provider_url><![CDATA[http://amphoteros.com]]></provider_url><author_name><![CDATA[ayudin2013]]></author_name><author_url><![CDATA[https://amphoteros.com/author/ayudin2013/]]></author_url><title><![CDATA[Thoughtful polarity arguments]]></title><type><![CDATA[link]]></type><html><![CDATA[<p>Last December, Dr. Steve Ritter of the <em>Chemical and Engineering News</em> asked me to comment on a paper from the lab of Prof. Petr Beier of the Czech Academy of Sciences. I gladly did (<a href="http://cen.acs.org/articles/94/web/2016/12/Fluorinated-azides-click-make-triazoles.html?type=paidArticleContent" rel="nofollow">http://cen.acs.org/articles/94/web/2016/12/Fluorinated-azides-click-make-triazoles.html?type=paidArticleContent</a>) and I just want to share my thoughts with you in the event you have not seen the Beier paper.</p>
<p>Every now and then we need a reminder of a rather straightforward kind: if we have trouble making a bond, just reverse the darn polarity of reagents! It is remarkable how infrequently this way of thinking pops into our heads, and I am judging from years of experience. Indeed, unless you are into radical reactions, there are always at least two ways to make a bond by a polar mechanism. In the example described by the Prague team in the <em>Angewandte</em> article, the curious CF<sub>3</sub>N<sub>3</sub> molecule was the target. Attempts to forge the C-N bond using CF<sub>3</sub>I as the electrophile led nowhere, whereas using the fluoroalkyl portion as the nucleophile delivered CF<sub>3</sub>N<sub>3 </sub>and other uncommon azides without a glitch. I know this stuff ultimately relates to the well-known umpolung arguments, but those of us who are in the business of making bonds would still rather search “closer to the lamp post” than reverse reagent polarity. I am convinced that there are a lot of other previously “unmakable” molecules that might be made using this simple logic. We should keep this in mind.</p>
<p><img data-attachment-id="4745" data-permalink="https://amphoteros.com/2017/01/24/thoughtful-polarity-arguments/22-8/" data-orig-file="https://amphoteros.files.wordpress.com/2017/01/22.jpg?w=1095&#038;h=250" data-orig-size="1095,250" data-comments-opened="1" data-image-meta="{&quot;aperture&quot;:&quot;0&quot;,&quot;credit&quot;:&quot;&quot;,&quot;camera&quot;:&quot;&quot;,&quot;caption&quot;:&quot;&quot;,&quot;created_timestamp&quot;:&quot;0&quot;,&quot;copyright&quot;:&quot;&quot;,&quot;focal_length&quot;:&quot;0&quot;,&quot;iso&quot;:&quot;0&quot;,&quot;shutter_speed&quot;:&quot;0&quot;,&quot;title&quot;:&quot;&quot;,&quot;orientation&quot;:&quot;0&quot;}" data-image-title="22" data-image-description="" data-medium-file="https://amphoteros.files.wordpress.com/2017/01/22.jpg?w=1095&#038;h=250?w=300" data-large-file="https://amphoteros.files.wordpress.com/2017/01/22.jpg?w=1095&#038;h=250?w=1024" class="alignnone size-full wp-image-4745" src="https://amphoteros.files.wordpress.com/2017/01/22.jpg?w=1095&#038;h=250" alt="22.jpg" width="1095" height="250" srcset="https://amphoteros.files.wordpress.com/2017/01/22.jpg 1095w, https://amphoteros.files.wordpress.com/2017/01/22.jpg?w=150&amp;h=34 150w, https://amphoteros.files.wordpress.com/2017/01/22.jpg?w=300&amp;h=68 300w, https://amphoteros.files.wordpress.com/2017/01/22.jpg?w=768&amp;h=175 768w, https://amphoteros.files.wordpress.com/2017/01/22.jpg?w=1024&amp;h=234 1024w" sizes="(max-width: 1095px) 100vw, 1095px" /></p>
<p style="text-align:center;"><a href="http://onlinelibrary.wiley.com/doi/10.1002/ange.201609715/abstract" rel="nofollow">http://onlinelibrary.wiley.com/doi/10.1002/ange.201609715/abstract</a></p>
]]></html><thumbnail_url><![CDATA[https://i1.wp.com/amphoteros.files.wordpress.com/2017/01/22.jpg?fit=440%2C330&ssl=1]]></thumbnail_url><thumbnail_width><![CDATA[438]]></thumbnail_width><thumbnail_height><![CDATA[100]]></thumbnail_height></oembed>