19860408

Source:http://linkedlifedata.com/resource/pubmed/id/19860408

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0001975, umls-concept:C0005068, umls-concept:C0007382, umls-concept:C0772162, umls-concept:C1522492
pubmed:issue	22
pubmed:dateCreated	2009-11-12
pubmed:abstractText	Ru-catalyzed cycloisomerizations of aromatic homo- and bis-homopropargylic alcohols effectively afford benzofurans and isochromenes. These processes proved to be chemo- and regioselective (5-, and 6-endo cyclizations) derived from key Ru vinylidene intermediates. The presence of an amine/ammonium base-acid pair is crucial for the catalytic cycle.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Nov
pubmed:issn	1523-7052
pubmed:author	pubmed-author:CastedoLuisL, pubmed-author:González-RodríguezCarlosC, pubmed-author:SaáCarlosC, pubmed-author:Varela-FernándezAlejandroA, pubmed-author:VarelaJesús AJA
pubmed:issnType	Electronic
pubmed:day	19
pubmed:volume	11
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5350-3
pubmed:year	2009
pubmed:articleTitle	Cycloisomerization of aromatic homo- and bis-homopropargylic alcohols via catalytic Ru vinylidenes: formation of benzofurans and isochromenes.
pubmed:affiliation	Departamento de Química Orgánica, Facultad de Química, Universidad de Santiago de Compostela, 15782 Santiago de Compostela, Spain.
pubmed:publicationType	Journal Article