12398526

Source:http://linkedlifedata.com/resource/pubmed/id/12398526

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0599473, umls-concept:C2699488
pubmed:issue	22
pubmed:dateCreated	2002-10-25
pubmed:abstractText	Reduction of (+/-)-5-chloro-5-methyl-2-cyclopentenone with BH(3).THF and catalytic (R)-2-methyl-CBS-oxazaborolidine gave readily separable diastereomers with high ee values. Oxidation of the diastereomers furnished the enantiomers of the chloromethylcyclopentenone.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/2985193R
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Nov
pubmed:issn	0022-3263
pubmed:author	pubmed-author:McMorrisTrevor CTC, pubmed-author:StaakeMichael DMD
pubmed:issnType	Print
pubmed:day	1
pubmed:volume	67
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	7902-3
pubmed:year	2002
pubmed:articleTitle	Resolution of both enantiomers of 5-chloro-5-methyl-2-cyclopentenone.
pubmed:affiliation	Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla 92093-0506, USA. tmcmorris@ucsd.edu
pubmed:publicationType	Journal Article