12841233

Source:http://linkedlifedata.com/resource/pubmed/id/12841233

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0002074, umls-concept:C0003075, umls-concept:C0443286
pubmed:issue	12
pubmed:dateCreated	2003-7-4
pubmed:abstractText	Lithiation and alkylation of a 2-isopropylidineaziridine bearing an (S)-alpha-methylbenzyl group on nitrogen proceeds with high levels of diastereocontrol (80-90% de).
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/9610838
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Jun
pubmed:issn	1359-7345
pubmed:author	pubmed-author:HayesJ FJF, pubmed-author:PrévostNN, pubmed-author:ProkesII, pubmed-author:RoweG DGD, pubmed-author:ShipmanMM, pubmed-author:SlawinA M ZAM
pubmed:issnType	Print
pubmed:day	21
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	1344-5
pubmed:year	2003
pubmed:articleTitle	Aziridinyl anions from a chiral, nonracemic 2-isopropylidineaziridine: surprisingly diastereoselective alkylation reactions.
pubmed:affiliation	GlaxoSmithKline, Old Powder Mills, Tonbridge, Kent, UK TN11 9AN.
pubmed:publicationType	Journal Article