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Article: Highly enantioselective carbonyl-ene reactions catalyzed by In(III)-PyBox complex

TitleHighly enantioselective carbonyl-ene reactions catalyzed by In(III)-PyBox complex
Authors
Issue Date2008
PublisherAmerican 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?
AbstractA 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 Identifierhttp://hdl.handle.net/10722/182335
ISSN
2021 Impact Factor: 16.383
2020 SCImago Journal Rankings: 7.115
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorZhao, JFen_US
dc.contributor.authorTsui, HYen_US
dc.contributor.authorWu, PJen_US
dc.contributor.authorLu, Jen_US
dc.contributor.authorLoh, TPen_US
dc.date.accessioned2013-04-23T08:18:59Z-
dc.date.available2013-04-23T08:18:59Z-
dc.date.issued2008en_US
dc.identifier.citationJournal Of The American Chemical Society, 2008, v. 130 n. 49, p. 16492-16493en_US
dc.identifier.issn0002-7863en_US
dc.identifier.urihttp://hdl.handle.net/10722/182335-
dc.description.abstractA 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.languageengen_US
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/jacsat/index.htmlen_US
dc.relation.ispartofJournal of the American Chemical Societyen_US
dc.subject.meshAlcohols - Chemistryen_US
dc.subject.meshCatalysisen_US
dc.subject.meshIndium - Chemistryen_US
dc.subject.meshMesylates - Chemistryen_US
dc.subject.meshOxazoles - Chemistryen_US
dc.subject.meshPyridines - Chemistryen_US
dc.subject.meshStereoisomerismen_US
dc.subject.meshSubstrate Specificityen_US
dc.titleHighly enantioselective carbonyl-ene reactions catalyzed by In(III)-PyBox complexen_US
dc.typeArticleen_US
dc.identifier.emailZhao, JF: zhao0065@e.ntu.edu.sgen_US
dc.identifier.authorityZhao, JF=rp01745en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1021/ja807501aen_US
dc.identifier.pmid19554724-
dc.identifier.scopuseid_2-s2.0-57549090773en_US
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-57549090773&selection=ref&src=s&origin=recordpageen_US
dc.identifier.volume130en_US
dc.identifier.issue49en_US
dc.identifier.spage16492en_US
dc.identifier.epage16493en_US
dc.identifier.isiWOS:000263320200025-
dc.publisher.placeUnited Statesen_US
dc.identifier.scopusauthoridZhao, JF=8393022100en_US
dc.identifier.scopusauthoridTsui, HY=36546988500en_US
dc.identifier.scopusauthoridWu, PJ=36547209200en_US
dc.identifier.scopusauthoridLu, J=36065866500en_US
dc.identifier.scopusauthoridLoh, TP=35234192600en_US
dc.identifier.issnl0002-7863-

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