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Article: Catalytic direct β-arylation of simple ketones with aryl iodides

TitleCatalytic direct β-arylation of simple ketones with aryl iodides
Authors
Issue Date2013
Citation
Journal of the American Chemical Society, 2013, v. 135, n. 47, p. 17747-17750 How to Cite?
AbstractHerein we report a direct β-arylation of simple ketones with widely available aryl iodides, combining palladium-catalyzed ketone oxidation, aryl-halide activation, and conjugate addition through a single catalytic cycle. Simple cyclic ketones with different ring-sizes, as well as acyclic ketones, can be directly arylated at the β-position with complete site-selectivity and excellent functional group tolerance. © 2013 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/276974
ISSN
2021 Impact Factor: 16.383
2020 SCImago Journal Rankings: 7.115
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorHuang, Zhongxing-
dc.contributor.authorDong, Guangbin-
dc.date.accessioned2019-09-18T08:35:13Z-
dc.date.available2019-09-18T08:35:13Z-
dc.date.issued2013-
dc.identifier.citationJournal of the American Chemical Society, 2013, v. 135, n. 47, p. 17747-17750-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10722/276974-
dc.description.abstractHerein we report a direct β-arylation of simple ketones with widely available aryl iodides, combining palladium-catalyzed ketone oxidation, aryl-halide activation, and conjugate addition through a single catalytic cycle. Simple cyclic ketones with different ring-sizes, as well as acyclic ketones, can be directly arylated at the β-position with complete site-selectivity and excellent functional group tolerance. © 2013 American Chemical Society.-
dc.languageeng-
dc.relation.ispartofJournal of the American Chemical Society-
dc.titleCatalytic direct β-arylation of simple ketones with aryl iodides-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ja410389a-
dc.identifier.scopuseid_2-s2.0-84889262891-
dc.identifier.volume135-
dc.identifier.issue47-
dc.identifier.spage17747-
dc.identifier.epage17750-
dc.identifier.eissn1520-5126-
dc.identifier.isiWOS:000328099400024-
dc.identifier.issnl0002-7863-

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