20000764

Source:http://linkedlifedata.com/resource/pubmed/id/20000764

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0014994, umls-concept:C0036140, umls-concept:C0043047, umls-concept:C0332514, umls-concept:C1883712
pubmed:issue	1
pubmed:dateCreated	2010-1-6
pubmed:abstractText	A novel strategy for the catalytic asymmetric Michael addition of aldehydes to nitroolefins on water has been developed and provided the Michael adducts in excellent diastereo- and enantioselectivities. A notable feature of these organocatalysts is that they can be recycled for more than six times without a significant loss of catalytic activity and stereochemical control. In addition, the synthetic procedure presented is simple, practical, and environmentally benign.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/7503056
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jan
pubmed:issn	1520-5126
pubmed:author	pubmed-author:NiBukuoB, pubmed-author:PerkinsBenjamin LBL, pubmed-author:ZhengZilongZ
pubmed:issnType	Electronic
pubmed:day	13
pubmed:volume	132
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	50-1
pubmed:year	2010
pubmed:articleTitle	Diarylprolinol silyl ether salts as new, efficient, water-soluble, and recyclable organocatalysts for the asymmetric Michael addition on water.
pubmed:affiliation	Department of Chemistry, Texas A&M University-Commerce, Commerce, Texas 75429-3011, USA.
pubmed:publicationType	Journal Article