12523833

Source:http://linkedlifedata.com/resource/pubmed/id/12523833

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0034255, umls-concept:C0037633, umls-concept:C0205390, umls-concept:C0443286, umls-concept:C1382100, umls-concept:C1516711
pubmed:issue	1
pubmed:dateCreated	2003-1-13
pubmed:abstractText	The 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.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100886263
pubmed:status	PubMed-not-MEDLINE
pubmed:issn	1520-4766
pubmed:author	pubmed-author:BagleyMark CMC, pubmed-author:BowerJustinJ, pubmed-author:DaleJames WJW, pubmed-author:OhnesorgeMarenM, pubmed-author:XiongXinX
pubmed:issnType	Print
pubmed:volume	5
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	41-4
pubmed:dateRevised	2003-11-4
pubmed:articleTitle	A facile solution phase combinatorial synthesis of tetrasubstituted pyridines using the Bohlmann-Rahtz heteroannulation reaction.
pubmed:affiliation	Department of Chemistry, Cardiff University, P.O. Box 912, Cardiff, CF10 3TB, United Kingdom. bagleymc@cf.ac.uk
pubmed:publicationType	Journal Article