http://rdf.ncbi.nlm.nih.gov/pubchem/reference/9958814

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contentType Journal Article
endingPage 107
issn 1477-9234
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issueIdentifier 8
pageRange 2098-107
publicationName Dalton transactions (Cambridge, England : 2003)
startingPage 2098
bibliographicCitation García JI, Jiménez-Osés G, López-Sánchez B, Mayoral JA, Vélez A. Stereoselectivity induced by support confinement effects. Aza-pyridinoxazolines: A new family of C(1)-symmetric ligands for copper-catalyzed enantioselective cyclopropanation reactions. Dalton Trans. 2010 Feb 27;39(8):2098–107. doi: 10.1039/b919274c. PMID: 20148230.
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date 2010-02-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://doi.org/10.1039/b919274c
https://pubmed.ncbi.nlm.nih.gov/20148230
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language English
source https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title Stereoselectivity induced by support confinement effects. Aza-pyridinoxazolines: A new family of C(1)-symmetric ligands for copper-catalyzed enantioselective cyclopropanation reactions

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isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128549565

Total number of triples: 26.