15278179

Source:http://linkedlifedata.com/resource/pubmed/id/15278179

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0038774, umls-concept:C0205117, umls-concept:C0220781, umls-concept:C0441587, umls-concept:C1883254
pubmed:issue	15
pubmed:dateCreated	2004-7-27
pubmed:abstractText	A new approach to the diastereoselective synthesis of thienofuranones is described in which an intramolecular 1,5-carbenoid C-H insertion adjacent to sulfur features as a key step.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Aug
pubmed:issn	1359-7345
pubmed:author	pubmed-author:BrownRichard C DRC, pubmed-author:BrutonGordonG, pubmed-author:HarrowvenDavid CDC, pubmed-author:SkerryPaul SPS, pubmed-author:SmythDonaldD, pubmed-author:SwainNigel ANA
pubmed:issnType	Print
pubmed:day	7
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1772-3
pubmed:year	2004
pubmed:articleTitle	Intramolecular C-H insertions adjacent to sulfur for the diastereoselective synthesis of thienofuranones.
pubmed:affiliation	Department of Chemistry, University of Southampton, Southampton SO17 1BJ, UK.
pubmed:publicationType	Journal Article