http://rdf.ncbi.nlm.nih.gov/pubchem/reference/1629753

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contentType Journal Article
endingPage 920
issn 1523-7052
1523-7060
issueIdentifier 6
pageRange 917-920
publicationName Organic Letters
startingPage 917
bibliographicCitation Rashatasakhon P, Ozdemir AD, Willis J, Padwa A. Six- versus five-membered ring formation in radical cyclizations of 7-bromo-substituted hexahydroindolinones. Org Lett. 2004 Mar 18;6(6):917–20. doi: 10.1021/ol036347z. PMID: 15012064.
creator http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_2128a1414204e0c984a67d5d55a32c12
http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_27933f1add20e17daf12a3fec3644c70
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http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0c008ef68c12b8c63f149c9209730475
date 2004-02-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier https://pubmed.ncbi.nlm.nih.gov/15012064
https://doi.org/10.1021/ol036347z
isPartOf http://rdf.ncbi.nlm.nih.gov/pubchem/journal/21677
https://portal.issn.org/resource/ISSN/1523-7052
https://portal.issn.org/resource/ISSN/1523-7060
language English
source https://www.crossref.org/
https://pubmed.ncbi.nlm.nih.gov/
title Six- versus Five-Membered Ring Formation in Radical Cyclizations of 7-Bromo-Substituted Hexahydroindolinones

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Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID248836003
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Total number of triples: 25.