<?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>Angewandte Chemie &#8211; BIOENGINEER.ORG</title>
	<atom:link href="https://bioengineer.org/tag/angewandte-chemie/feed/" rel="self" type="application/rss+xml" />
	<link>https://bioengineer.org</link>
	<description>Bioengineering</description>
	<lastBuildDate>Thu, 08 Oct 2026 15:44:01 +0000</lastBuildDate>
	<language>en-US</language>
	<sy:updatePeriod>
	hourly	</sy:updatePeriod>
	<sy:updateFrequency>
	1	</sy:updateFrequency>
	<generator>https://wordpress.org/?v=7.1.3</generator>

<image>
	<url>https://bioengineer.org/wp-content/uploads/2019/09/cropped-bioengineering-32x32.png</url>
	<title>Angewandte Chemie &#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>Nickel Catalyst Uses Halogen Bonds to Deliver Elusive Anti-β-Amino Alcohols</title>
		<link>https://bioengineer.org/nickel-catalyst-uses-halogen-bonds-to-deliver-elusive-anti-%ce%b2-amino-alcohols/</link>
		
		<dc:creator><![CDATA[]]></dc:creator>
		<pubDate>Thu, 08 Oct 2026 15:44:01 +0000</pubDate>
				<category><![CDATA[Chemistry]]></category>
		<category><![CDATA[Angewandte Chemie]]></category>
		<category><![CDATA[artificial metalloenzymes]]></category>
		<category><![CDATA[Chiba University]]></category>
		<category><![CDATA[enantioselective synthesis]]></category>
		<category><![CDATA[halogen bonding]]></category>
		<category><![CDATA[Henry reaction]]></category>
		<category><![CDATA[hydrogen bonding]]></category>
		<category><![CDATA[nickel catalyst]]></category>
		<category><![CDATA[organocatalysis]]></category>
		<category><![CDATA[pharmaceutical building blocks]]></category>
		<category><![CDATA[Stereochemistry]]></category>
		<category><![CDATA[β-amino alcohols]]></category>
		<guid isPermaLink="false">https://bioengineer.org/?p=407793</guid>

					<description><![CDATA[Researchers at Chiba University have developed a chiral nickel catalyst that uses cooperating halogen bonds, hydrogen bonds, and metal coordination to synthesize hard-to-make anti-β-amino alcohols with exceptional selectivity.]]></description>
		
		
		
		<post-id xmlns="com-wordpress:feed-additions:1">407793</post-id>	</item>
	</channel>
</rss>
