reference/23412535

Predicate	Object
contentType	Journal Article
endingPage	5355
issn	1523-7052 1523-7060
issueIdentifier	23
pageRange	5353-5355
publicationName	Organic Letters
startingPage	5353
bibliographicCitation	Scholtis S, Ide A, Mahrwald R. Enantioselective equilibration-access to chiral aldol adducts of mandelic acid esters. Org Lett. 2006 Nov 09;8(23):5353–5. doi: 10.1021/ol062252w. PMID: 17078716.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0c46a28f516fcbf4e5769925a07e7eb3 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_344763b16bf5fd39753c9b1c16c520a0 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_e9c60f43df38927cd568c34b863a29ea
date	2006-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://doi.org/10.1021/ol062252w https://pubmed.ncbi.nlm.nih.gov/17078716
isPartOf	http://rdf.ncbi.nlm.nih.gov/pubchem/journal/21677 https://portal.issn.org/resource/ISSN/1523-7060 https://portal.issn.org/resource/ISSN/1523-7052
language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Enantioselective Equilibration−Access to Chiral Aldol Adducts of Mandelic Acid Esters
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID2733945 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4374 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6451515

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127866917 http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID127746861

Total number of triples: 27.