<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:wfw="http://wellformedweb.org/CommentAPI/"
	xmlns:dc="http://purl.org/dc/elements/1.1/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Higher diamondoids &#8211; BIOENGINEER.ORG</title>
	<atom:link href="https://bioengineer.org/tag/higher-diamondoids/feed/" rel="self" type="application/rss+xml" />
	<link>https://bioengineer.org</link>
	<description>Bioengineering</description>
	<lastBuildDate>Tue, 06 Jan 2026 20:42:49 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.0</generator>

<image>
	<url>https://bioengineer.org/wp-content/uploads/2019/09/cropped-bioengineering-32x32.png</url>
	<title>Higher diamondoids &#8211; BIOENGINEER.ORG</title>
	<link>https://bioengineer.org</link>
	<width>32</width>
	<height>32</height>
</image> 
<site xmlns="com-wordpress:feed-additions:1">72741379</site>	<item>
		<title>Stereoselective Total Synthesis of Skew-Tetramantane Achieved</title>
		<link>https://bioengineer.org/stereoselective-total-synthesis-of-skew-tetramantane-achieved/</link>
		
		<dc:creator><![CDATA[Bioengineer]]></dc:creator>
		<pubDate>Tue, 06 Jan 2026 20:42:44 +0000</pubDate>
				<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[Adamantane-based cages]]></category>
		<category><![CDATA[Higher diamondoids]]></category>
		<category><![CDATA[Nanomaterials applications]]></category>
		<category><![CDATA[Skew-tetramantane]]></category>
		<category><![CDATA[stereoselective synthesis]]></category>
		<guid isPermaLink="false">https://bioengineer.org/stereoselective-total-synthesis-of-skew-tetramantane-achieved/</guid>

					<description><![CDATA[In a groundbreaking advancement poised to redefine the landscape of synthetic chemistry, researchers Li and Sparr have unveiled a stereoselective total synthesis of a complex diamondoid structure known as (P)-skew-tetramantane. Published in Nature Chemistry, this seminal work introduces a methodical extension of adamantane-based cage molecules, effectively opening a gateway to the systematic generation of higher [&#8230;]]]></description>
		
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">314228</post-id>	</item>
	</channel>
</rss>
