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pubmed-article:12523833rdf:typepubmed:Citationlld:pubmed
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pubmed-article:12523833pubmed:issue1lld:pubmed
pubmed-article:12523833pubmed:dateCreated2003-1-13lld:pubmed
pubmed-article:12523833pubmed:abstractTextThe solution phase combinatorial Bohlmann-Rahtz reaction gives highly functionalized pyridine libraries from enamino esters and alkynones in a single synthetic step. Good product ratios and library purities were obtained in reactions catalyzed by zinc(II) bromide, the acid-catalyzed heteroannulation procedure offering considerable improvements over traditional methodology.lld:pubmed
pubmed-article:12523833pubmed:languageenglld:pubmed
pubmed-article:12523833pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12523833pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:12523833pubmed:issn1520-4766lld:pubmed
pubmed-article:12523833pubmed:authorpubmed-author:BagleyMark...lld:pubmed
pubmed-article:12523833pubmed:authorpubmed-author:DaleJames WJWlld:pubmed
pubmed-article:12523833pubmed:authorpubmed-author:BowerJustinJlld:pubmed
pubmed-article:12523833pubmed:authorpubmed-author:OhnesorgeMare...lld:pubmed
pubmed-article:12523833pubmed:authorpubmed-author:XiongXinXlld:pubmed
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pubmed-article:12523833pubmed:volume5lld:pubmed
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pubmed-article:12523833pubmed:pagination41-4lld:pubmed
pubmed-article:12523833pubmed:dateRevised2003-11-4lld:pubmed
pubmed-article:12523833pubmed:articleTitleA facile solution phase combinatorial synthesis of tetrasubstituted pyridines using the Bohlmann-Rahtz heteroannulation reaction.lld:pubmed
pubmed-article:12523833pubmed:affiliationDepartment of Chemistry, Cardiff University, P.O. Box 912, Cardiff, CF10 3TB, United Kingdom. bagleymc@cf.ac.uklld:pubmed
pubmed-article:12523833pubmed:publicationTypeJournal Articlelld:pubmed