15255745

Source:http://linkedlifedata.com/resource/pubmed/id/15255745

Download in:

Switch to

Custom View

Named Graph Language Inference

Statements in which the resource exists as a subject.
Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0185125, umls-concept:C0205314, umls-concept:C0220781, umls-concept:C0449444, umls-concept:C0679622, umls-concept:C1883254
pubmed:issue	15
pubmed:dateCreated	2004-7-16
pubmed:abstractText	Reactions of secondary amides 2a-i with 1-chloro-1H-benzotriazole and triphenylphosphine give imidoylbenzotriazoles 3a-i. The treatment of 3a,b,e,g with silyl enol ethers 5a,b in the presence of potassium tert-butoxide provides a new general approach to enaminoketones 6a-h.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jul
pubmed:issn	0022-3263
pubmed:author	pubmed-author:GohJ YJY, pubmed-author:HaydenAmy EAE, pubmed-author:KatritzkyAlan RAR, pubmed-author:KirichenkoKostyantynK, pubmed-author:PelphreyPhillipP
pubmed:issnType	Print
pubmed:day	23
pubmed:volume	69
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5108-11
pubmed:year	2004
pubmed:articleTitle	A novel route to imidoylbenzotriazoles and their application for the synthesis of enaminones.
pubmed:affiliation	Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, FL 32611-7200, USA. katritzky@chem.ufl.edu
pubmed:publicationType	Journal Article