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- Publisher Website: 10.1021/ja807501a
- Scopus: eid_2-s2.0-57549090773
- PMID: 19554724
- WOS: WOS:000263320200025
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Article: Highly enantioselective carbonyl-ene reactions catalyzed by In(III)-PyBox complex
Title | Highly enantioselective carbonyl-ene reactions catalyzed by In(III)-PyBox complex |
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Authors | |
Issue Date | 2008 |
Publisher | American Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/jacsat/index.html |
Citation | Journal Of The American Chemical Society, 2008, v. 130 n. 49, p. 16492-16493 How to Cite? |
Abstract | A highly enantioselective carbonyl-ene reaction catalyzed by In(III)-pybox is described. Both 1,1-disubstituted alkenes and 1,1,2-trisubstituted alkenes proceeded smoothly to give the ene products in high yields up to 97% and with excellent diastereoselectivity and enantioselectivities up to >99:1 and 99%, respectively. Copyright © 2008 American Chemical Society. |
Persistent Identifier | http://hdl.handle.net/10722/182335 |
ISSN | 2023 Impact Factor: 14.4 2023 SCImago Journal Rankings: 5.489 |
ISI Accession Number ID | |
References |
DC Field | Value | Language |
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dc.contributor.author | Zhao, JF | en_US |
dc.contributor.author | Tsui, HY | en_US |
dc.contributor.author | Wu, PJ | en_US |
dc.contributor.author | Lu, J | en_US |
dc.contributor.author | Loh, TP | en_US |
dc.date.accessioned | 2013-04-23T08:18:59Z | - |
dc.date.available | 2013-04-23T08:18:59Z | - |
dc.date.issued | 2008 | en_US |
dc.identifier.citation | Journal Of The American Chemical Society, 2008, v. 130 n. 49, p. 16492-16493 | en_US |
dc.identifier.issn | 0002-7863 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/182335 | - |
dc.description.abstract | A highly enantioselective carbonyl-ene reaction catalyzed by In(III)-pybox is described. Both 1,1-disubstituted alkenes and 1,1,2-trisubstituted alkenes proceeded smoothly to give the ene products in high yields up to 97% and with excellent diastereoselectivity and enantioselectivities up to >99:1 and 99%, respectively. Copyright © 2008 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/jacsat/index.html | en_US |
dc.relation.ispartof | Journal of the American Chemical Society | en_US |
dc.subject.mesh | Alcohols - Chemistry | en_US |
dc.subject.mesh | Catalysis | en_US |
dc.subject.mesh | Indium - Chemistry | en_US |
dc.subject.mesh | Mesylates - Chemistry | en_US |
dc.subject.mesh | Oxazoles - Chemistry | en_US |
dc.subject.mesh | Pyridines - Chemistry | en_US |
dc.subject.mesh | Stereoisomerism | en_US |
dc.subject.mesh | Substrate Specificity | en_US |
dc.title | Highly enantioselective carbonyl-ene reactions catalyzed by In(III)-PyBox complex | en_US |
dc.type | Article | en_US |
dc.identifier.email | Zhao, JF: zhao0065@e.ntu.edu.sg | en_US |
dc.identifier.authority | Zhao, JF=rp01745 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1021/ja807501a | en_US |
dc.identifier.pmid | 19554724 | - |
dc.identifier.scopus | eid_2-s2.0-57549090773 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-57549090773&selection=ref&src=s&origin=recordpage | en_US |
dc.identifier.volume | 130 | en_US |
dc.identifier.issue | 49 | en_US |
dc.identifier.spage | 16492 | en_US |
dc.identifier.epage | 16493 | en_US |
dc.identifier.isi | WOS:000263320200025 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Zhao, JF=8393022100 | en_US |
dc.identifier.scopusauthorid | Tsui, HY=36546988500 | en_US |
dc.identifier.scopusauthorid | Wu, PJ=36547209200 | en_US |
dc.identifier.scopusauthorid | Lu, J=36065866500 | en_US |
dc.identifier.scopusauthorid | Loh, TP=35234192600 | en_US |
dc.identifier.issnl | 0002-7863 | - |