11772076

Source:http://linkedlifedata.com/resource/pubmed/id/11772076

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0010546, umls-concept:C0439807, umls-concept:C0441513, umls-concept:C0470187, umls-concept:C1527177, umls-concept:C1709634
pubmed:issue	1
pubmed:dateCreated	2002-1-4
pubmed:abstractText	[reaction: see text] beta-Hydroxyalkyl aryl chalcogenides, readily available by regioselective ring-opening of epoxides with nucleophilic benzeneselenolate or tellurolate, were O-alkylated by treatment with ethyl propiolate or (E)-1,2-bis(phenylsulfonyl)ethylene. Subsequent carbonylation/reductive cyclization in the presence of AIBN/TTMSS and carbon monoxide (80 atm) afforded tetrahydrofuran-3-ones in moderate to good yields.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jan
pubmed:issn	1523-7060
pubmed:author	pubmed-author:BerlinStefanS, pubmed-author:EngmanLarsL, pubmed-author:EricssonCeciliaC
pubmed:issnType	Print
pubmed:day	10
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3-6
pubmed:dateRevised	2003-10-31
pubmed:year	2002
pubmed:articleTitle	Construction of tetrahydrofuran-3-ones from readily available organochalcogen precursors via radical carbonylation/reductive cyclization.
pubmed:affiliation	Uppsala University, Institute of Chemistry, Department of Organic Chemistry, Box 531, S-751 21, Uppsala, Sweden.
pubmed:publicationType	Journal Article