20157778

Source:http://linkedlifedata.com/resource/pubmed/id/20157778

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0039856, umls-concept:C0220781, umls-concept:C1519249, umls-concept:C1883254
pubmed:issue	3
pubmed:dateCreated	2010-11-18
pubmed:abstractText	2,4-Disubstituted benzo[b][1,5]thiazepines represent nonfluorescent intense yellow chromophores and are readily synthesized from acid chlorides, terminal alkynes, and ortho-amino thiophenols by a consecutive one-pot three-component Sonogashira coupling-Michael addition-cyclocondensation sequence under mild conditions in good yields.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9516534
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/1,5-benzothiazepine, http://linkedlifedata.com/resource/pubmed/chemical/Thiazepines
pubmed:status	MEDLINE
pubmed:month	Aug
pubmed:issn	1573-501X
pubmed:author	pubmed-author:MüllerThomas J JTJ, pubmed-author:WillyBenjaminB
pubmed:issnType	Electronic
pubmed:volume	14
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	443-53
pubmed:meshHeading	pubmed-meshheading:20157778-Chemistry, Organic, pubmed-meshheading:20157778-Cyclization, pubmed-meshheading:20157778-Models, Molecular, pubmed-meshheading:20157778-Spectrometry, Mass, Matrix-Assisted Laser..., pubmed-meshheading:20157778-Spectrophotometry, Ultraviolet, pubmed-meshheading:20157778-Thiazepines
pubmed:year	2010
pubmed:articleTitle	Three-component synthesis of benzo[b][1,5]thiazepines via coupling-addition-cyclocondensation sequence.
pubmed:affiliation	Institut für Organische Chemie und Makromolekulare Chemie, Heinrich-Heine-Universität Düsseldorf, Universitätsstraße 1, 40225 Düsseldorf, Germany.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't