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	<title>Comments on: Carvone (You can smell chirality!)</title>
	<link>http://www.moleculeoftheday.com/2006/05/12/carvone-you-can-smell-chirality/</link>
	<description>Molecules: You'd Better Learn to Live With Them</description>
	<pubDate>Sat, 22 Nov 2008 01:54:57 +0000</pubDate>
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		<title>by: Molecule of the Day &#187; Blog Archive &#187; Grapefruit Mercaptan (Not all sulfur stinks)</title>
		<link>http://www.moleculeoftheday.com/2006/05/12/carvone-you-can-smell-chirality/#comment-2763</link>
		<pubDate>Tue, 01 Aug 2006 00:38:28 +0000</pubDate>
		<guid>http://www.moleculeoftheday.com/2006/05/12/carvone-you-can-smell-chirality/#comment-2763</guid>
					<description>[...] All this leads up to a truly unusual thiol: grapefruit mercaptan. You&amp;#8217;ll notice it looks like another terpene, like carvone and damascone. Grapefruit mercaptan is such a singular compound because it is a nice-smelling thiol. It&amp;#8217;s another one I haven&amp;#8217;t smelled, but I&amp;#8217;m told it&amp;#8217;s very complex and grapefruity. It&amp;#8217;s also unique because not many things synthesize thiols on purpose (thiols being reactive and stinky - skunks are a notable exception here). [...]</description>
		<content:encoded><![CDATA[<p>[&#8230;] All this leads up to a truly unusual thiol: grapefruit mercaptan. You&#8217;ll notice it looks like another terpene, like carvone and damascone. Grapefruit mercaptan is such a singular compound because it is a nice-smelling thiol. It&#8217;s another one I haven&#8217;t smelled, but I&#8217;m told it&#8217;s very complex and grapefruity. It&#8217;s also unique because not many things synthesize thiols on purpose (thiols being reactive and stinky - skunks are a notable exception here). [&#8230;]
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		<title>by: Carl E. Bond Biology of Fishes &#187; laimalt</title>
		<link>http://www.moleculeoftheday.com/2006/05/12/carvone-you-can-smell-chirality/#comment-24</link>
		<pubDate>Wed, 17 May 2006 13:41:51 +0000</pubDate>
		<guid>http://www.moleculeoftheday.com/2006/05/12/carvone-you-can-smell-chirality/#comment-24</guid>
					<description>[...] Carvone (You can smell chirality!) [...]</description>
		<content:encoded><![CDATA[<p>[&#8230;] Carvone (You can smell chirality!) [&#8230;]
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		<title>by: Molecule of the Day &#187; Blog Archive &#187; Isopentenyl Pyrophosphate (Or, One Kind of Biomolecular Legos)</title>
		<link>http://www.moleculeoftheday.com/2006/05/12/carvone-you-can-smell-chirality/#comment-21</link>
		<pubDate>Tue, 16 May 2006 01:58:10 +0000</pubDate>
		<guid>http://www.moleculeoftheday.com/2006/05/12/carvone-you-can-smell-chirality/#comment-21</guid>
					<description>[...] Friday, we talked about about carvone. I mentioned that it comes from the same biosynthetic pathway as cholesterol. The precursor to this, as well as a number of other natural products, is isopentenyl pyrophosphate, which we&amp;#8217;ll refer to as IPP: [...]</description>
		<content:encoded><![CDATA[<p>[&#8230;] Friday, we talked about about carvone. I mentioned that it comes from the same biosynthetic pathway as cholesterol. The precursor to this, as well as a number of other natural products, is isopentenyl pyrophosphate, which we&#8217;ll refer to as IPP: [&#8230;]
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		<title>by: Stuart</title>
		<link>http://www.moleculeoftheday.com/2006/05/12/carvone-you-can-smell-chirality/#comment-20</link>
		<pubDate>Fri, 12 May 2006 11:00:57 +0000</pubDate>
		<guid>http://www.moleculeoftheday.com/2006/05/12/carvone-you-can-smell-chirality/#comment-20</guid>
					<description>I would always use limonene as the example, one enantiomer smells of oranges, the other, lemons...</description>
		<content:encoded><![CDATA[<p>I would always use limonene as the example, one enantiomer smells of oranges, the other, lemons&#8230;
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