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- Publisher Website: 10.1021/ol900355h
- Scopus: eid_2-s2.0-66149101004
- PMID: 19338292
- WOS: WOS:000265529000012
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Article: Palladium-Catalyzed highly diastereoselective oxidative cascade cyclization reactions
Title | Palladium-Catalyzed highly diastereoselective oxidative cascade cyclization reactions |
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Authors | |
Issue Date | 2009 |
Publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html |
Citation | Organic Letters, 2009, v. 11 n. 9, p. 1911-1914 How to Cite? |
Abstract | Isoquinoline and quinoline have been discovered as novel ligands for palladium-catalyzed oxidative cascade cyclization reactions. With our new catalyst systems (Pd(OAc)2/isoquinoline or quinoline), unsaturated anilides cyclize under an oxygen atmosphere (1 atm) to furnish structurally versatile indoline derivatives in good yields. One C-N bond and two C-C bonds are formed in a single step with excellent diastereoselectivities (dr> 24:1). © 2009 American Chemical Society. |
Persistent Identifier | http://hdl.handle.net/10722/168378 |
ISSN | 2023 Impact Factor: 4.9 2023 SCImago Journal Rankings: 1.245 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Yip, KT | en_HK |
dc.contributor.author | Zhu, NY | en_HK |
dc.contributor.author | Yang, D | en_HK |
dc.date.accessioned | 2012-10-08T03:18:12Z | - |
dc.date.available | 2012-10-08T03:18:12Z | - |
dc.date.issued | 2009 | en_HK |
dc.identifier.citation | Organic Letters, 2009, v. 11 n. 9, p. 1911-1914 | en_HK |
dc.identifier.issn | 1523-7060 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/168378 | - |
dc.description.abstract | Isoquinoline and quinoline have been discovered as novel ligands for palladium-catalyzed oxidative cascade cyclization reactions. With our new catalyst systems (Pd(OAc)2/isoquinoline or quinoline), unsaturated anilides cyclize under an oxygen atmosphere (1 atm) to furnish structurally versatile indoline derivatives in good yields. One C-N bond and two C-C bonds are formed in a single step with excellent diastereoselectivities (dr> 24:1). © 2009 American Chemical Society. | en_HK |
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_HK |
dc.relation.ispartof | Organic Letters | en_HK |
dc.title | Palladium-Catalyzed highly diastereoselective oxidative cascade cyclization reactions | en_HK |
dc.type | Article | en_HK |
dc.identifier.email | Yip, KT: billyyip@graduate.hku.hk | en_HK |
dc.identifier.email | Zhu, NY: nzhu@hkucc.hku.hk | en_HK |
dc.identifier.email | Yang, D: yangdan@hku.hk | en_HK |
dc.identifier.authority | Yip, KT=rp00832 | en_HK |
dc.identifier.authority | Zhu, NY=rp00845 | en_HK |
dc.identifier.authority | Yang, D=rp00825 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1021/ol900355h | en_HK |
dc.identifier.pmid | 19338292 | - |
dc.identifier.scopus | eid_2-s2.0-66149101004 | en_HK |
dc.identifier.hkuros | 160416 | - |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-66149101004&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 11 | en_HK |
dc.identifier.issue | 9 | en_HK |
dc.identifier.spage | 1911 | en_HK |
dc.identifier.epage | 1914 | en_HK |
dc.identifier.isi | WOS:000265529000012 | - |
dc.publisher.place | United States | en_HK |
dc.identifier.scopusauthorid | Yip, KT=10440172200 | en_HK |
dc.identifier.scopusauthorid | Zhu, NY=7201449530 | en_HK |
dc.identifier.scopusauthorid | Yang, D=7404800756 | en_HK |
dc.identifier.issnl | 1523-7052 | - |