20234921

Source:http://linkedlifedata.com/resource/pubmed/id/20234921

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0022634, umls-concept:C0043902, umls-concept:C0075804, umls-concept:C0205250, umls-concept:C0220781, umls-concept:C0303781, umls-concept:C0348080, umls-concept:C1883254
pubmed:issue	13
pubmed:dateCreated	2010-3-17
pubmed:abstractText	A new Vilsmeier reagent-mediated Nazarov cyclization-halovinylation reaction of divinyl ketones was developed to provide a straightforward method for the synthesis of highly substituted cyclopentadienes with the advantages of simplicity of execution, readily available substrates, cheap reagents, and broad range of potential products and applications.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Apr
pubmed:issn	1364-548X
pubmed:author	pubmed-author:EninV MVM, pubmed-author:OKAM JMJ, pubmed-author:WangMangM, pubmed-author:YuanHongjuanH
pubmed:issnType	Electronic
pubmed:day	7
pubmed:volume	46
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2247-9
pubmed:year	2010
pubmed:articleTitle	Tandem Nazarov cyclization-halovinylation of divinyl ketones under Vilsmeier conditions: synthesis of highly substituted cyclopentadienes.
pubmed:affiliation	Department of Chemistry, Northeast Normal University, Changchun 130024, China. wangm452@nenu.edu.cn
pubmed:publicationType	Journal Article