11796057

Source:http://linkedlifedata.com/resource/pubmed/id/11796057

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0243072, umls-concept:C1260969, umls-concept:C1883254
pubmed:issue	2
pubmed:dateCreated	2002-1-17
pubmed:abstractText	[reaction: see text] Various 1-arylnaphthalenes, including highly substituted derivatives, are accessible via a simple two-step process. Treatment of alkenylbenzocyclobutenones with aryllithium provides two-carbon expanded dihydronaphthalenes, which are readily dehydrated by MsCl-Et(3)N or PPTS in MeOH.
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:HamuraToshiyukiT, pubmed-author:MatsumotoTakashiT, pubmed-author:MiyamotoMakotoM, pubmed-author:SuzukiKeisukeK
pubmed:issnType	Print
pubmed:day	24
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	229-32
pubmed:dateRevised	2003-10-31
pubmed:year	2002
pubmed:articleTitle	Synthesis of hindered 1-arylnaphthalene derivatives via ring expansion of benzocyclobutenones.
pubmed:affiliation	Department of Chemistry, Tokyo Institute of Technology, and CREST, Japan Science and Technology (JST) Corporation, O-okayama, Meguro-ku, Tokyo 152-8551, Japan.
pubmed:publicationType	Journal Article