<?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[Done with surgical&nbsp;precision]]></title><type><![CDATA[link]]></type><html><![CDATA[<p>I was asked to write a perspective on macrocycles for <em>Chemical Science</em>, which is why I am in the mood for some interesting nuggets this field is loaded with. I hope that the examples I choose will convince the readers that they are in for a big surprise if they think that cyclic peptides are essentially peptides, only cyclic. This is very far away from the truth, but let me use a specific example. What if I gave you a molecule shown below and asked you to invert the stereocenter that is circled from <em>S</em> into <em>R</em>? I cannot see how there would be an intuitively clear answer to this question. However, there is a set of simple conditions that effect this transformation. This chemistry is detailed in a cool paper published in <em>Synlett</em> by Oberhauser and co-workers from Novartis. If you read this work, you will note that there is a clear explanation for why this particular stereocenter is special. By the way, if you feel compelled to share an interesting facet of macrocycle chemistry with me, I will appreciate your insights.</p>
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<p style="text-align:center;"><a href="https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-1999-3103" rel="nofollow">https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-1999-3103</a></p>
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