File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1002/anie.201100044
- Scopus: eid_2-s2.0-79955760094
- PMID: 21538740
- WOS: WOS:000290664400029
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Efficient gold(I)-catalyzed direct intramolecular hydroalkylation of unactivated alkenes with α-ketones
| Title | Efficient gold(I)-catalyzed direct intramolecular hydroalkylation of unactivated alkenes with α-ketones | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Authors | |||||||||||||
| Keywords | cyclic compounds gold homogeneous catalysis hydroalkylation unactivated alkenes | ||||||||||||
| Issue Date | 2011 | ||||||||||||
| 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, 2011, v. 50 n. 21, p. 4937-4941 How to Cite? | ||||||||||||
| Abstract | Easy access by gold: The Au I-catalyzed title reaction provides simple and efficient access to highly substituted cyclic compounds with excellent yields and good diastereoselectivity. This transformation constitutes the first example of transition-metal-catalyzed direct hydroalkylation of unactivated alkenes with simple α-ketone groups in the absence of additive reagents. Bn=benzyl, Ts=tosyl. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | ||||||||||||
| Persistent Identifier | http://hdl.handle.net/10722/134352 | ||||||||||||
| ISSN | 2023 Impact Factor: 16.1 2023 SCImago Journal Rankings: 5.300 | ||||||||||||
| ISI Accession Number ID |
Funding Information: We are thankful for the financial support of The University of Hong Kong (University Development Fund), the Hong Kong Research Grants Council, and the University Grants Committee of the Hong Kong SAR of China (Area of Excellence Scheme, AoE/P-10/01). Y.-P.X. thanks the Croucher Foundation of Hong Kong and the External Cooperation Program of CAS (GJHZ200816). | ||||||||||||
| References | |||||||||||||
| Grants |
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Xiao, YP | en_HK |
| dc.contributor.author | Liu, XY | en_HK |
| dc.contributor.author | Che, CM | en_HK |
| dc.date.accessioned | 2011-06-17T09:18:29Z | - |
| dc.date.available | 2011-06-17T09:18:29Z | - |
| dc.date.issued | 2011 | en_HK |
| dc.identifier.citation | Angewandte Chemie - International Edition, 2011, v. 50 n. 21, p. 4937-4941 | en_HK |
| dc.identifier.issn | 1433-7851 | en_HK |
| dc.identifier.uri | http://hdl.handle.net/10722/134352 | - |
| dc.description.abstract | Easy access by gold: The Au I-catalyzed title reaction provides simple and efficient access to highly substituted cyclic compounds with excellent yields and good diastereoselectivity. This transformation constitutes the first example of transition-metal-catalyzed direct hydroalkylation of unactivated alkenes with simple α-ketone groups in the absence of additive reagents. Bn=benzyl, Ts=tosyl. Copyright © 2011 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | en_HK |
| 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_HK |
| dc.relation.ispartof | Angewandte Chemie - International Edition | en_HK |
| dc.subject | cyclic compounds | en_HK |
| dc.subject | gold | en_HK |
| dc.subject | homogeneous catalysis | en_HK |
| dc.subject | hydroalkylation | en_HK |
| dc.subject | unactivated alkenes | en_HK |
| dc.title | Efficient gold(I)-catalyzed direct intramolecular hydroalkylation of unactivated alkenes with α-ketones | en_HK |
| dc.type | Article | en_HK |
| dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1433-7851&volume=50&issue=21&spage=4937&epage=4941&date=2011&atitle=Efficient+gold(I)-catalyzed+direct+intramolecular+hydroalkylation+of+unactivated+alkenes+with+α-ketones | - |
| dc.identifier.email | Che, CM:cmche@hku.hk | en_HK |
| dc.identifier.authority | Che, CM=rp00670 | en_HK |
| dc.description.nature | link_to_subscribed_fulltext | - |
| dc.identifier.doi | 10.1002/anie.201100044 | en_HK |
| dc.identifier.pmid | 21538740 | - |
| dc.identifier.scopus | eid_2-s2.0-79955760094 | en_HK |
| dc.identifier.hkuros | 185602 | en_US |
| dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-79955760094&selection=ref&src=s&origin=recordpage | en_HK |
| dc.identifier.volume | 50 | en_HK |
| dc.identifier.issue | 21 | en_HK |
| dc.identifier.spage | 4937 | en_HK |
| dc.identifier.epage | 4941 | en_HK |
| dc.identifier.isi | WOS:000290664400029 | - |
| dc.publisher.place | Germany | en_HK |
| dc.relation.project | Institute of molecular technology for drug discovery and synthesis | - |
| dc.identifier.scopusauthorid | Xiao, YP=7403260506 | en_HK |
| dc.identifier.scopusauthorid | Liu, XY=48662515100 | en_HK |
| dc.identifier.scopusauthorid | Che, CM=7102442791 | en_HK |
| dc.identifier.issnl | 1433-7851 | - |