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- Publisher Website: 10.1021/ol202609a
- Scopus: eid_2-s2.0-80955133311
- PMID: 22013883
- WOS: WOS:000296756600046
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Article: Palladium-catalyzed decarboxylative coupling of isatoic anhydrides with arylboronic acids
Title | Palladium-catalyzed decarboxylative coupling of isatoic anhydrides with arylboronic acids |
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Authors | |
Issue Date | 2011 |
Publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html |
Citation | Organic Letters, 2011, v. 13 n. 22, p. 6114-6117 How to Cite? |
Abstract | The decarboxylative coupling of isatoic anhydrides with arylboronic acids was realized for the first time in the presence of Pd 2(dba) 3 and DPEphos, achieving aryl o-aminobenzoates with yields ranging from moderate to good. The efficiency of this procedure was demonstrated by good compatibility with fluoro, chloro, bromo, nitro, cyano, trifluoromethyl, formacyl, acetyl, thienyl, and naphthyl groups. Preliminary mechanistic experiments using deuterium labeling showed that the oxygen atom was derived from dioxygen. © 2011 American Chemical Society. |
Persistent Identifier | http://hdl.handle.net/10722/168584 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.245 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Lu, W | en_US |
dc.contributor.author | Chen, J | en_US |
dc.contributor.author | Liu, M | en_US |
dc.contributor.author | Ding, J | en_US |
dc.contributor.author | Gao, W | en_US |
dc.contributor.author | Wu, H | en_US |
dc.date.accessioned | 2012-10-08T03:21:06Z | - |
dc.date.available | 2012-10-08T03:21:06Z | - |
dc.date.issued | 2011 | en_US |
dc.identifier.citation | Organic Letters, 2011, v. 13 n. 22, p. 6114-6117 | en_US |
dc.identifier.issn | 1523-7060 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/168584 | - |
dc.description.abstract | The decarboxylative coupling of isatoic anhydrides with arylboronic acids was realized for the first time in the presence of Pd 2(dba) 3 and DPEphos, achieving aryl o-aminobenzoates with yields ranging from moderate to good. The efficiency of this procedure was demonstrated by good compatibility with fluoro, chloro, bromo, nitro, cyano, trifluoromethyl, formacyl, acetyl, thienyl, and naphthyl groups. Preliminary mechanistic experiments using deuterium labeling showed that the oxygen atom was derived from dioxygen. © 2011 American Chemical Society. | en_US |
dc.language | eng | en_US |
dc.publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html | en_US |
dc.relation.ispartof | Organic Letters | en_US |
dc.subject.mesh | Alkylation | en_US |
dc.subject.mesh | Boronic Acids - Chemistry | en_US |
dc.subject.mesh | Carboxylic Acids - Chemistry | en_US |
dc.subject.mesh | Catalysis | en_US |
dc.subject.mesh | Molecular Structure | en_US |
dc.subject.mesh | Oxazines - Chemistry | en_US |
dc.subject.mesh | Oxygen - Chemistry | en_US |
dc.subject.mesh | Palladium - Chemistry | en_US |
dc.title | Palladium-catalyzed decarboxylative coupling of isatoic anhydrides with arylboronic acids | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lu, W:luwei@hku.hk | en_US |
dc.identifier.authority | Lu, W=rp00754 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1021/ol202609a | en_US |
dc.identifier.pmid | 22013883 | - |
dc.identifier.scopus | eid_2-s2.0-80955133311 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-80955133311&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 13 | en_US |
dc.identifier.issue | 22 | en_US |
dc.identifier.spage | 6114 | en_US |
dc.identifier.epage | 6117 | en_US |
dc.identifier.isi | WOS:000296756600046 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Lu, W=27868087600 | en_US |
dc.identifier.scopusauthorid | Chen, J=12798105400 | en_US |
dc.identifier.scopusauthorid | Liu, M=7406298559 | en_US |
dc.identifier.scopusauthorid | Ding, J=8420084800 | en_US |
dc.identifier.scopusauthorid | Gao, W=35299177700 | en_US |
dc.identifier.scopusauthorid | Wu, H=35301460100 | en_US |
dc.identifier.citeulike | 10074918 | - |
dc.identifier.issnl | 1523-7052 | - |