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	<title>ChemNews.Org</title>
	<link>http://chemnews.org/en</link>
	<description>News of Organic Chemistry</description>
	<pubDate>Mon, 02 Nov 2009 19:41:34 +0000</pubDate>
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		<title>Расщепление двойных связей</title>
		<link>http://chemnews.org/en/?p=174</link>
		<comments>http://chemnews.org/en/?p=174#comments</comments>
		<pubDate>Mon, 02 Nov 2009 19:36:22 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[_]]></category>

		<guid isPermaLink="false">http://chemnews.org/en/?p=174</guid>
		<description><![CDATA[

Окисление перманганатом калия и бихроматом калия в кислой среде:
 R2C=CHR  →  R2C=O + RCOOH
 
Деградация по Барбье-Виланду (на один атом углерода):


 
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		<item>
		<title>Окисление диоксидом селена</title>
		<link>http://chemnews.org/en/?p=163</link>
		<comments>http://chemnews.org/en/?p=163#comments</comments>
		<pubDate>Mon, 02 Nov 2009 19:21:49 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[_]]></category>

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		<description><![CDATA[




  

Окисление кетонов в дикетоны:



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		<item>
		<title>Расщепление двойных связей: озонолиз</title>
		<link>http://chemnews.org/en/?p=147</link>
		<comments>http://chemnews.org/en/?p=147#comments</comments>
		<pubDate>Sat, 19 Sep 2009 14:23:57 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
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]]></description>
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		<title>Дегидрирование</title>
		<link>http://chemnews.org/en/?p=146</link>
		<comments>http://chemnews.org/en/?p=146#comments</comments>
		<pubDate>Sat, 19 Sep 2009 14:23:55 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[_]]></category>

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		<description><![CDATA[ 

Ароматизация происходит легче, если уже есть двойные связи.
]]></description>
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		<item>
		<title>Окисление сульфидов и аренов</title>
		<link>http://chemnews.org/en/?p=145</link>
		<comments>http://chemnews.org/en/?p=145#comments</comments>
		<pubDate>Sat, 19 Sep 2009 14:23:54 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
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		<description><![CDATA[Окисление сульфидов



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		<item>
		<title>Окисление альдегидов</title>
		<link>http://chemnews.org/en/?p=144</link>
		<comments>http://chemnews.org/en/?p=144#comments</comments>
		<pubDate>Sat, 19 Sep 2009 14:23:52 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[_]]></category>

		<guid isPermaLink="false">http://chemnews.org/en/?p=144</guid>
		<description><![CDATA[

Окислители: KMnO4 в кислой, щелочной и нейтральной среде, H2CrO4, Br2, O2.
]]></description>
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		<item>
		<title>Расщепление гликолей</title>
		<link>http://chemnews.org/en/?p=143</link>
		<comments>http://chemnews.org/en/?p=143#comments</comments>
		<pubDate>Sat, 19 Sep 2009 14:16:57 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[_]]></category>

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]]></description>
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		<item>
		<title>Окисление спиртов - 2</title>
		<link>http://chemnews.org/en/?p=142</link>
		<comments>http://chemnews.org/en/?p=142#comments</comments>
		<pubDate>Sat, 19 Sep 2009 14:13:36 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
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		<description><![CDATA[Окисление по Корнблюму:


]]></description>
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		<item>
		<title>Окисление спиртов</title>
		<link>http://chemnews.org/en/?p=141</link>
		<comments>http://chemnews.org/en/?p=141#comments</comments>
		<pubDate>Sat, 19 Sep 2009 14:10:13 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[_]]></category>

		<guid isPermaLink="false">http://chemnews.org/en/?p=141</guid>
		<description><![CDATA[


Окислители: K2Cr2O7, Na2Cr2O7 (лучше растворим в воде), H2SO4, KMnO4, Br2, MnO2.

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		<item>
		<title>Scope of a Novel Three-Component Synthesis of Highly Functionalized Pyridines</title>
		<link>http://chemnews.org/en/?p=101</link>
		<comments>http://chemnews.org/en/?p=101#comments</comments>
		<pubDate>Fri, 18 Sep 2009 09:57:26 +0000</pubDate>
		<dc:creator>admin</dc:creator>
		
		<category><![CDATA[Heterocycles]]></category>

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		<description><![CDATA[A mechanistically unique provides a variety of functionalized pyridine derivatives in fair to excellent yields. The scope of this reaction was studied with respect to the alkoxyallene, the nitrile, and the carboxylic acid.



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