12599456

Source:http://linkedlifedata.com/resource/pubmed/id/12599456

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0007382, umls-concept:C0014630, umls-concept:C0051225, umls-concept:C0205314, umls-concept:C0679622, umls-concept:C2699488
pubmed:issue	22
pubmed:dateCreated	2003-2-25
pubmed:abstractText	[formula: see text] The kinetic resolution of racemic epoxides via catalytic enantioselective rearrangement to allylic alcohols was investigated. Using the Li-salt of (1S,3R,4R)-3-(pyrrolidinyl)methyl-2-azabicyclo [2.2.1] heptane 1 as catalyst allowed both epoxides and allylic alcohols to be obtained in an enantioenriched form.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/100890393
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Oct
pubmed:issn	1523-7060
pubmed:author	pubmed-author:AnderssonPher GPG, pubmed-author:BertilssonSophieS, pubmed-author:GayetArnaudA
pubmed:issnType	Print
pubmed:day	31
pubmed:volume	4
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	3777-9
pubmed:dateRevised	2003-11-4
pubmed:year	2002
pubmed:articleTitle	Novel catalytic kinetic resolution of racemic epoxides to allylic alcohols.
pubmed:affiliation	Department of Organic Chemistry, Institute of Chemistry, Uppsala University, Box 531, S-751 21 Uppsala, Sweden.
pubmed:publicationType	Journal Article