16465335

Source:http://linkedlifedata.com/resource/pubmed/id/16465335

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0175892
pubmed:issue	7
pubmed:dateCreated	2006-2-8
pubmed:abstractText	An unexpected, mild, efficient bromination ring-opening method has been developed for convenient synthesis of various novel biladienes or brominated porphyrins by controlling the amounts of NBS used.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/Bromine, http://linkedlifedata.com/resource/pubmed/chemical/Porphyrins
pubmed:status	MEDLINE
pubmed:month	Feb
pubmed:issn	1359-7345
pubmed:author	pubmed-author:ChenQing-YunQY, pubmed-author:LiuChaoC, pubmed-author:ShenDong-MeiDM
pubmed:issnType	Print
pubmed:day	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	770-2
pubmed:meshHeading	pubmed-meshheading:16465335-Bromine, pubmed-meshheading:16465335-Models, Chemical, pubmed-meshheading:16465335-Models, Molecular, pubmed-meshheading:16465335-Porphyrins, pubmed-meshheading:16465335-Stereoisomerism
pubmed:year	2006
pubmed:articleTitle	Unexpected bromination ring-opening of tetraarylporphyrins.
pubmed:affiliation	Key Laboratory of Organofluorine Chemistry, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, 354 Fenglin Road, 200032, China.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't