11300856

Source:http://linkedlifedata.com/resource/pubmed/id/11300856

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0013682, umls-concept:C0040880, umls-concept:C0053250, umls-concept:C0441833, umls-concept:C1707455, umls-concept:C1707959
pubmed:issue	2
pubmed:dateCreated	2001-4-13
pubmed:abstractText	Three polymer-supported heterocyclic (triazole 4 and benzotriazoles 2, 8) leaving groups are described. The loading of 8 was clearly superior to those of 2 and 4. The efficiency of 8 was higher than those of previously reported benzotriazole resins 9a,b in the C-acylation of ketones.
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:KatritzkyA RAR, pubmed-author:PastorAA, pubmed-author:TymoshenkoDD, pubmed-author:VoronkovMM
pubmed:issnType	Print
pubmed:volume	3
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	167-70
pubmed:dateRevised	2003-10-31
pubmed:articleTitle	Polymer-supported triazole and benzotriazole leaving groups. Three new examples and a comparison of their efficiency.
pubmed:affiliation	Department of Chemistry, Center for Heterocyclic Compounds, University of Florida, Gainesville, Florida 32611-7200, USA.
pubmed:publicationType	Journal Article