<?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[On early mornings without coffee (but with&nbsp;boron)]]></title><type><![CDATA[link]]></type><html><![CDATA[<p>Yesterday morning I was doodling on a piece of paper, thinking about Zhi’s synthesis of alpha boryl aldehydes. These molecules offer a nice entry into boron-containing intermediates (I blogged about them in July). Of course, &#8220;B&#8221; stands for &#8220;boron&#8221;&#8230;</p>
<p>It was early in the a.m., I did not have my coffee yet, and I somehow typed bromine (Br) instead of boron (B)… But then it occurred to me: “crap, there is something weirdly familiar here!”. I started digging into our old papers and I found one by my former PhD student Larissa Krasnova from 2006. She developed this nice hydrazone formation:</p>
<p><a href="http://pubs.acs.org/doi/abs/10.1021/ol061695x?prevSearch=%255BContrib%253A%2Bkrasnova%255D&#038;searchHistoryKey=" rel="nofollow">http://pubs.acs.org/doi/abs/10.1021/ol061695x?prevSearch=%255BContrib%253A%2Bkrasnova%255D&#038;searchHistoryKey=</a></p>
<p>If you compare her work to our boryl aldehyde synthesis, there is an interesting parallel in terms of what migrates and what is around the migrating group&#8230; Mechanisms are different, but still:</p>
<p><a href="https://amphoteros.files.wordpress.com/2013/08/boron-and-bromine.jpg"><img class="size-full wp-image aligncenter" id="i-318" alt="Image" src="https://amphoteros.files.wordpress.com/2013/08/boron-and-bromine.jpg?w=487" srcset="https://amphoteros.files.wordpress.com/2013/08/boron-and-bromine.jpg?w=487 487w, https://amphoteros.files.wordpress.com/2013/08/boron-and-bromine.jpg?w=974 974w, https://amphoteros.files.wordpress.com/2013/08/boron-and-bromine.jpg?w=150 150w, https://amphoteros.files.wordpress.com/2013/08/boron-and-bromine.jpg?w=300 300w, https://amphoteros.files.wordpress.com/2013/08/boron-and-bromine.jpg?w=768 768w" sizes="(max-width: 487px) 100vw, 487px" /></a></p>
<p>Whenever there are interesting ways of comparing the incomparable, I always go back to the lessons taught to us by Roald Hoffmann of Cornell. I refer to isolobal relationships, of course.</p>
<p>In our case there is no isolobal relationship, just a lack of caffeine, but still&#8230; Interesting.</p>
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