reference/30456702

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/30456702

Outgoing Links

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endingPage	11590
issn	1433-7851 1521-3773
issueIdentifier	28
pageRange	11583-11590
publicationName	Angewandte Chemie (International ed. in English)
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bibliographicCitation	Lv S, Han X, Wang JY, Zhou M, Wu Y, Ma L, Niu L, Gao W, Zhou J, Hu W, Cui Y, Chen J. Tunable Electrochemical C-N versus N-N Bond Formation of Nitrogen-Centered Radicals Enabled by Dehydrogenative Dearomatization: Biological Applications. Angew Chem Int Ed Engl. 2020 Jul 06;59(28):11583–90. doi: 10.1002/anie.202001510. PMID: 32203637.
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date	2020-04-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/32203637 https://doi.org/10.1002/anie.202001510
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	Tunable Electrochemical C−N versus N−N Bond Formation of Nitrogen‐Centered Radicals Enabled by Dehydrogenative Dearomatization: Biological Applications
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Total number of triples: 56.