reference/3158987

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contentType	Journal Article
endingPage	6559
issn	1523-7060 1523-7052
issueIdentifier	24
pageRange	6556-6559
publicationName	Organic Letters
startingPage	6556
bibliographicCitation	Štacko P, Šolomek T, Klán P. Electronic-state switching strategy in the photochemical synthesis of indanones from o-methyl phenacyl epoxides. Org Lett. 2011 Dec 16;13(24):6556–9. doi: 10.1021/ol202892r. PMID: 22091870.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_05e6e830b005aba4f7a7c1f63e1c16a4 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_d6a6184c3edb130e2e659993f698b310 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0003-0013-4116 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_7683d3e7f5d51d8cee912256929dd874 http://rdf.ncbi.nlm.nih.gov/pubchem/author/ORCID_0000-0001-6287-2742
date	2011-11-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/22091870 https://doi.org/10.1021/ol202892r
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	Electronic-State Switching Strategy in the Photochemical Synthesis of Indanones from o-Methyl Phenacyl Epoxides
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Total number of triples: 30.