21607242

Source:http://linkedlifedata.com/resource/pubmed/id/21607242

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0020276, umls-concept:C0699795, umls-concept:C1261512, umls-concept:C1269765, umls-concept:C1304680, umls-concept:C1879547
pubmed:issue	25
pubmed:dateCreated	2011-6-15
pubmed:abstractText	The possibility of tunable regioselective activation of a dinitrile towards nucleophilic attack was demonstrated. For that, a sulfo-arylhydrazone unit was introduced into malononitrile and the thus formed intramolecular hydrogen bond systems assisted specific nucleophilic attacks to the cyano moieties leading to a variety of amidines, carboxamides and iminoesters depending on the nucleophiles and conditions used.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jul
pubmed:issn	1364-548X
pubmed:author	pubmed-author:KopylovichMaximilian NMN, pubmed-author:MahmudovKamran TKT, pubmed-author:MizarArchanaA, pubmed-author:PombeiroArmando J LAJ
pubmed:copyrightInfo	This journal is © The Royal Society of Chemistry 2011
pubmed:issnType	Electronic
pubmed:day	7
pubmed:volume	47
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	7248-50
pubmed:year	2011
pubmed:articleTitle	Hydrogen bond assisted activation of a dinitrile towards nucleophilic attack.
pubmed:affiliation	Centro Química Estrutural, Complexo I, Instituto Superior Técnico, TU Lisbon, Av. Rovisco Pais, 1049-001, Lisbon, Portugal.
pubmed:publicationType	Journal Article