12839470

Source:http://linkedlifedata.com/resource/pubmed/id/12839470

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0021242, umls-concept:C0034325
pubmed:issue	14
pubmed:dateCreated	2003-7-3
pubmed:abstractText	In a new general indole synthesis, the anion derived from benzotriazolyl derivative 5b underwent regioselective 1,4-addition to various alpha,beta-unsaturated ketones; subsequent acid-catalyzed cyclization formed the corresponding indoles 1a-f.
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:KatritzkyAlan RAR, pubmed-author:LedouxStephaneS, pubmed-author:NairSatheesh KSK
pubmed:issnType	Print
pubmed:day	11
pubmed:volume	68
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	5728-30
pubmed:year	2003
pubmed:articleTitle	Benzannulation of 3-substituted pyrroles to indoles.
pubmed:affiliation	Center for Heterocyclic Compounds, Department of Chemistry, University of Florida, Gainesville, Florida 32611-7200, USA. katritzky@chem.ufl.edu
pubmed:publicationType	Journal Article