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Article: Ligand-enabled methylene C(sp3)-H bond activation with a Pd(II) catalyst

TitleLigand-enabled methylene C(sp3)-H bond activation with a Pd(II) catalyst
Authors
Wasa, MasayukiChan, Kelvin S.L.Zhang, Xing GuoHe, JianMiura, MasanoriYu, Jin Quan
Issue Date2012
Citation
Journal of the American Chemical Society, 2012, v. 134, n. 45, p. 18570-18572 How to Cite?
DOI: http://dx.doi.org/10.1021/ja309325e
AbstractPd(II) insertion into β-methylene C(sp3)-H bonds was enabled by a mutually repulsive and electron-rich quinoline ligand. Ligand tuning led to the development of a method that allows for installation of an aryl group on a range of acyclic and cyclic amides containing β-methylene C(sp3)-H bonds. © 2012 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/276939
ISSN
0002-7863
2021 Impact Factor: 16.383
2020 SCImago Journal Rankings: 7.115
ISI Accession Number ID
WOS:000311192100024

 

DC FieldValueLanguage
dc.contributor.authorWasa, Masayuki-
dc.contributor.authorChan, Kelvin S.L.-
dc.contributor.authorZhang, Xing Guo-
dc.contributor.authorHe, Jian-
dc.contributor.authorMiura, Masanori-
dc.contributor.authorYu, Jin Quan-
dc.date.accessioned2019-09-18T08:35:07Z-
dc.date.available2019-09-18T08:35:07Z-
dc.date.issued2012-
dc.identifier.citationJournal of the American Chemical Society, 2012, v. 134, n. 45, p. 18570-18572-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10722/276939-
dc.description.abstractPd(II) insertion into β-methylene C(sp3)-H bonds was enabled by a mutually repulsive and electron-rich quinoline ligand. Ligand tuning led to the development of a method that allows for installation of an aryl group on a range of acyclic and cyclic amides containing β-methylene C(sp3)-H bonds. © 2012 American Chemical Society.-
dc.languageeng-
dc.relation.ispartofJournal of the American Chemical Society-
dc.titleLigand-enabled methylene C(sp3)-H bond activation with a Pd(II) catalyst-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ja309325e-
dc.identifier.pmid23116159-
dc.identifier.scopuseid_2-s2.0-84869456845-
dc.identifier.volume134-
dc.identifier.issue45-
dc.identifier.spage18570-
dc.identifier.epage18572-
dc.identifier.eissn1520-5126-
dc.identifier.isiWOS:000311192100024-
dc.identifier.issnl0002-7863-

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