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				<datestamp>2012-08-06T14:50:19Z</datestamp>
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	<dc:title xml:lang="en-US">Recent progress in the asymmetric Mannich reaction</dc:title>
	<dc:creator>Xiao-Hua, Cai</dc:creator>
	<dc:creator>Hui, Guo</dc:creator>
	<dc:creator>Bing, Xie</dc:creator>
	<dc:subject xml:lang="en-US">Chiral amine catalysis</dc:subject>
	<dc:subject xml:lang="en-US">Chiral Bronsted acid</dc:subject>
	<dc:subject xml:lang="en-US">Asymmetric organocatalysis</dc:subject>
	<dc:subject xml:lang="en-US">Metal-based organocatalysis</dc:subject>
	<dc:subject xml:lang="en-US">Asymmetric Mannich reaction</dc:subject>
	<dc:subject xml:lang="en-US">Diastereo- and enantioselective</dc:subject>
	<dc:description xml:lang="en-US">The asymmetric Mannich reaction is one of the most useful carbon-carbon bond forming reactions for the synthesis of chiral molecules containing nitrogen. The resulting β-amino carbonyl compounds are valuable synthons in the preparation of many natural products with useful biological properties. In recent years, asymmetric Mannich processes have increasingly been reported and used in a rapidly growing number of applications. This review provides an overview of the recent history of the applications of various catalytic systems in asymmetric Mannich reaction, including metal-based asymmetric organocatalysis, asymmetric organocatalysis, other chiral catalysis and no chiral catalysis systems.</dc:description>
	<dc:publisher xml:lang="en-US">Atlanta Publishing House LLC</dc:publisher>
	<dc:date>2012-06-30</dc:date>
	<dc:type>info:eu-repo/semantics/article</dc:type>
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	<dc:identifier>https://www.eurjchem.com/index.php/eurjchem/article/view/536</dc:identifier>
	<dc:identifier>10.5155/eurjchem.3.2.258-266.536</dc:identifier>
	<dc:source xml:lang="en-US">European Journal of Chemistry; Vol. 3 No. 2 (2012): June 2012; 258-266</dc:source>
	<dc:source>2153-2257</dc:source>
	<dc:source>2153-2249</dc:source>
	<dc:language>eng</dc:language>
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