18047359

Source:http://linkedlifedata.com/resource/pubmed/id/18047359

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010546, umls-concept:C0205250, umls-concept:C0220781, umls-concept:C0443286, umls-concept:C1883254
pubmed:issue	26
pubmed:dateCreated	2007-12-13
pubmed:abstractText	A convenient and efficient synthesis of highly substituted pyrrolin-4-ones is developed via the PIFA-mediated cyclization reactions of readily available enaminones, and a mechanism involving sequential cleavage of N-C bond, formation of new N-C bond, intramolecular addition reaction, and benzilic acid type rearrangement is proposed.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Dec
pubmed:issn	1523-7060
pubmed:author	pubmed-author:DongDewenD, pubmed-author:HuangJieJ, pubmed-author:LiangYongjiuY, pubmed-author:XXX, pubmed-author:YinP HPH
pubmed:issnType	Print
pubmed:day	20
pubmed:volume	9
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5345-8
pubmed:year	2007
pubmed:articleTitle	Efficient synthesis of highly substituted Pyrrolin-4-ones via PIFA-mediated cyclization reactions of enaminones.
pubmed:affiliation	Department of Chemistry, Northeast Normal University, Changchun 130024, China.
pubmed:publicationType	Journal Article