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- Publisher Website: 10.1002/anie.200805383
- Scopus: eid_2-s2.0-70349784860
- PMID: 19212999
- WOS: WOS:000264784400022
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Article: Highly efficient and regioselective platinum(II)-Catalyzed tandem synthesisof multiply substituted indolines and tetrahydro-Quinolines
| Title | Highly efficient and regioselective platinum(II)-Catalyzed tandem synthesisof multiply substituted indolines and tetrahydro-Quinolines |
|---|---|
| Authors | |
| Keywords | 1,3-Diketones Aminoalkynes Cyclization Platinum Synthetic Methods |
| Issue Date | 2009 |
| Publisher | Wiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home |
| Citation | Angewandte Chemie - International Edition, 2009, v. 48 n. 13, p. 2367-2371 How to Cite? |
| Abstract | A special advantage: The platinum(II)-catalyzed tandem cyclization of aminoalkynes with 1,3-diketones offers a new and highly efficient method for the synthesis of indolines and tetrahydroquinolines (see scheme; M.S.=molecular sieves). This transformation affords good to excellent product yields with high regio- and chemoselectivity under mild reaction conditions. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA. |
| Persistent Identifier | http://hdl.handle.net/10722/168408 |
| ISSN | 2021 Impact Factor: 16.823 2020 SCImago Journal Rankings: 5.831 |
| ISI Accession Number ID | |
| References |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Liu, XY | en_US |
| dc.contributor.author | Che, CM | en_US |
| dc.date.accessioned | 2012-10-08T03:18:35Z | - |
| dc.date.available | 2012-10-08T03:18:35Z | - |
| dc.date.issued | 2009 | en_US |
| dc.identifier.citation | Angewandte Chemie - International Edition, 2009, v. 48 n. 13, p. 2367-2371 | en_US |
| dc.identifier.issn | 1433-7851 | en_US |
| dc.identifier.uri | http://hdl.handle.net/10722/168408 | - |
| dc.description.abstract | A special advantage: The platinum(II)-catalyzed tandem cyclization of aminoalkynes with 1,3-diketones offers a new and highly efficient method for the synthesis of indolines and tetrahydroquinolines (see scheme; M.S.=molecular sieves). This transformation affords good to excellent product yields with high regio- and chemoselectivity under mild reaction conditions. © 2009 Wiley-VCH Verlag GmbH & Co. KGaA. | en_US |
| dc.language | eng | en_US |
| dc.publisher | Wiley - V C H Verlag GmbH & Co. KGaA. The Journal's web site is located at http://www3.interscience.wiley.com/journal/26737/home | en_US |
| dc.relation.ispartof | Angewandte Chemie - International Edition | en_US |
| dc.subject | 1,3-Diketones | en_US |
| dc.subject | Aminoalkynes | en_US |
| dc.subject | Cyclization | en_US |
| dc.subject | Platinum | en_US |
| dc.subject | Synthetic Methods | en_US |
| dc.title | Highly efficient and regioselective platinum(II)-Catalyzed tandem synthesisof multiply substituted indolines and tetrahydro-Quinolines | en_US |
| dc.type | Article | en_US |
| dc.identifier.email | Che, CM:cmche@hku.hk | en_US |
| dc.identifier.authority | Che, CM=rp00670 | en_US |
| dc.description.nature | link_to_subscribed_fulltext | en_US |
| dc.identifier.doi | 10.1002/anie.200805383 | - |
| dc.identifier.pmid | 19212999 | - |
| dc.identifier.scopus | eid_2-s2.0-70349784860 | en_US |
| dc.identifier.hkuros | 155983 | - |
| dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-70349784860&selection=ref&src=s&origin=recordpage | en_US |
| dc.identifier.volume | 48 | en_US |
| dc.identifier.issue | 13 | en_US |
| dc.identifier.spage | 2367 | en_US |
| dc.identifier.epage | 2371 | en_US |
| dc.identifier.isi | WOS:000264784400022 | - |
| dc.publisher.place | Germany | en_US |
| dc.identifier.scopusauthorid | Liu, XY=27171788000 | en_US |
| dc.identifier.scopusauthorid | Che, CM=7102442791 | en_US |
| dc.identifier.issnl | 1433-7851 | - |