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- Publisher Website: 10.1002/ejoc.201201070
- Scopus: eid_2-s2.0-84869005779
- WOS: WOS:000310981500013
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Article: Auto-tandem catalysis: Synthesis of acridines by Pd-catalyzed C=C bond formation and C(sp2)-N cross-coupling
Title | Auto-tandem catalysis: Synthesis of acridines by Pd-catalyzed C=C bond formation and C(sp2)-N cross-coupling |
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Authors | |
Keywords | Cross-coupling Palladium Nitrogen heterocycles Homogeneous catalysis Cyclization Auto-tandem catalysis |
Issue Date | 2012 |
Citation | European Journal of Organic Chemistry, 2012, n. 33, p. 6586-6593 How to Cite? |
Abstract | A facile palladium-catalyzed synthesis of acridines has been realized by consecutive C=C double bond formation and C-N cross-coupling. A variety of functionalized acridines can be accessed from easily available o-dihalobenzenes and N-tosylhydrazones in a single operation. This one-pot protocol has a wide scope with respect to both coupling partners, and provides an efficient route to functionalized acridine derivatives, which are generally difficult to synthesize by previously known methods. © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Persistent Identifier | http://hdl.handle.net/10722/276937 |
ISSN | 2023 Impact Factor: 2.5 2023 SCImago Journal Rankings: 0.584 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Huang, Zhongxing | - |
dc.contributor.author | Yang, Yang | - |
dc.contributor.author | Xiao, Qing | - |
dc.contributor.author | Zhang, Yan | - |
dc.contributor.author | Wang, Jianbo | - |
dc.date.accessioned | 2019-09-18T08:35:06Z | - |
dc.date.available | 2019-09-18T08:35:06Z | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | European Journal of Organic Chemistry, 2012, n. 33, p. 6586-6593 | - |
dc.identifier.issn | 1434-193X | - |
dc.identifier.uri | http://hdl.handle.net/10722/276937 | - |
dc.description.abstract | A facile palladium-catalyzed synthesis of acridines has been realized by consecutive C=C double bond formation and C-N cross-coupling. A variety of functionalized acridines can be accessed from easily available o-dihalobenzenes and N-tosylhydrazones in a single operation. This one-pot protocol has a wide scope with respect to both coupling partners, and provides an efficient route to functionalized acridine derivatives, which are generally difficult to synthesize by previously known methods. © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. | - |
dc.language | eng | - |
dc.relation.ispartof | European Journal of Organic Chemistry | - |
dc.subject | Cross-coupling | - |
dc.subject | Palladium | - |
dc.subject | Nitrogen heterocycles | - |
dc.subject | Homogeneous catalysis | - |
dc.subject | Cyclization | - |
dc.subject | Auto-tandem catalysis | - |
dc.title | Auto-tandem catalysis: Synthesis of acridines by Pd-catalyzed C=C bond formation and C(sp2)-N cross-coupling | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/ejoc.201201070 | - |
dc.identifier.scopus | eid_2-s2.0-84869005779 | - |
dc.identifier.issue | 33 | - |
dc.identifier.spage | 6586 | - |
dc.identifier.epage | 6593 | - |
dc.identifier.eissn | 1099-0690 | - |
dc.identifier.isi | WOS:000310981500013 | - |
dc.identifier.issnl | 1099-0690 | - |