reference/31633386

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contentType	Journal Article
endingPage	10819
issn	1521-3773 1433-7851
issueIdentifier	43
pageRange	10816-10819
publicationName	Angewandte Chemie (International ed. in English)
startingPage	10816
bibliographicCitation	Nakamura I, Okamoto M, Sato Y, Terada M. Synthesis of azepine derivatives by rhodium-catalyzed tandem 2,3-rearrangement/heterocyclization. Angew Chem Int Ed Engl. 2012 Oct 22;51(43):10816–9. doi: 10.1002/anie.201205285. PMID: 22936441.
creator	http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_09b31d708374176bc463579e7a73d849 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_0d01fbca20b66ac9e9f9157fafc8ec52 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_362979be88c783743f07a8c7df43fa85 http://rdf.ncbi.nlm.nih.gov/pubchem/author/MD5_4382426af6384ff1ef9966b652d9d44c
date	2012-08-31-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/22936441 https://doi.org/10.1002/anie.201205285
isPartOf	https://portal.issn.org/resource/ISSN/1521-3773 https://portal.issn.org/resource/ISSN/1433-7851 http://rdf.ncbi.nlm.nih.gov/pubchem/journal/537
language	English
source	https://www.crossref.org/ https://pubmed.ncbi.nlm.nih.gov/
title	Synthesis of Azepine Derivatives by Rhodium‐Catalyzed Tandem 2,3‐Rearrangement/Heterocyclization
discussesAsDerivedByTextMining	http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6451476 http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID23948

Predicate	Subject
isDiscussedBy	http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID323505213 http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129461805

Total number of triples: 27.