19436917

Source:http://linkedlifedata.com/resource/pubmed/id/19436917

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0311404, umls-concept:C0439810, umls-concept:C0915026, umls-concept:C0917735, umls-concept:C1522240, umls-concept:C1883254
pubmed:issue	20
pubmed:dateCreated	2009-5-13
pubmed:abstractText	A concise total synthesis of (+/-)-aspidospermidine has been achieved in twelve steps from inexpensive 4-ethylphenol, based on an oxidative Hosomi-Sakurai reaction via the concept of "aromatic ring umpolung".
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:citationSubset	IM
pubmed:chemical	http://linkedlifedata.com/resource/pubmed/chemical/4-ethylphenol, http://linkedlifedata.com/resource/pubmed/chemical/Indole Alkaloids, http://linkedlifedata.com/resource/pubmed/chemical/Phenols, http://linkedlifedata.com/resource/pubmed/chemical/Quinolines, http://linkedlifedata.com/resource/pubmed/chemical/aspidospermidine
pubmed:status	MEDLINE
pubmed:month	May
pubmed:issn	1359-7345
pubmed:author	pubmed-author:CanesiSylvainS, pubmed-author:GuérardKimiaka CKC, pubmed-author:SabotCyrilleC
pubmed:issnType	Print
pubmed:day	28
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	2941-3
pubmed:meshHeading	pubmed-meshheading:19436917-Indole Alkaloids, pubmed-meshheading:19436917-Isomerism, pubmed-meshheading:19436917-Oxidation-Reduction, pubmed-meshheading:19436917-Phenols, pubmed-meshheading:19436917-Quinolines
pubmed:year	2009
pubmed:articleTitle	Concise total synthesis of (+/-)-aspidospermidine via an oxidative Hosomi-Sakurai process.
pubmed:affiliation	Laboratoire de Méthodologie et Synthèse de Produits Naturels, Université du Québec à Montréal, Montréal, Québec, Canada.
pubmed:publicationType	Journal Article, Research Support, Non-U.S. Gov't