11170253

Source:http://linkedlifedata.com/resource/pubmed/id/11170253

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Predicate	Object
rdf:type	pubmed:Citation
lifeskim:mentions	umls-concept:C0220781, umls-concept:C0443286, umls-concept:C1883254
pubmed:issue	2
pubmed:dateCreated	2001-2-22
pubmed:abstractText	2-Bromoesters enriched in the (S,R)-diastereoisomer can be easily prepared by coupling of racemic 2-bromoacids with (R)-pantolactone. Displacement of the bromine atom with nucleophiles, under suitable reaction conditions, occurs without epimerization of starting compounds, giving (R,R)-2-substituted carboxylic acid derivatives.
pubmed:language	eng
pubmed:journal	http://linkedlifedata.com/resource/pubmed/journal/8914261
pubmed:status	PubMed-not-MEDLINE
pubmed:month	Feb
pubmed:issn	0899-0042
pubmed:author	pubmed-author:AmmazzalorsoAA, pubmed-author:AmorosoRR, pubmed-author:BettoniGG, pubmed-author:FilippisBB
pubmed:copyrightInfo	Copyright 2001 Wiley-Liss, Inc.
pubmed:issnType	Print
pubmed:volume	13
pubmed:owner	NLM
pubmed:authorsComplete	Y
pubmed:pagination	102-8
pubmed:dateRevised	2003-10-31
pubmed:year	2001
pubmed:articleTitle	Synthesis of diastereomerically enriched 2-bromoesters and their reaction with nucleophiles.
pubmed:affiliation	Dipartimento di Scienze del Farmaco, Università "G. D'Annunzio," Chieti, Italy.
pubmed:publicationType	Journal Article