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Article: A Three-Component Reaction toward the Synthesis of 1-Carboxamido-isoindoles

TitleA Three-Component Reaction toward the Synthesis of 1-Carboxamido-isoindoles
Authors
Zhang, YLee, CLLiu, HLi, X
Issue Date2012
PublisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html
Citation
Organic Letters, 2012, v. 14 n. 19, p. 5146-5149 How to Cite?
DOI: http://dx.doi.org/10.1021/ol302460s
AbstractAn efficient three-component reaction toward the facile synthesis of structurally diverse 1-carboxamido-isoindoles has been developed. The resultant isoindoles can be used in Diels-Alder reactions.
Persistent Identifierhttp://hdl.handle.net/10722/185682
ISSN
1523-7060
2021 Impact Factor: 6.072
2020 SCImago Journal Rankings: 1.940
ISI Accession Number ID
WOS:000309438400043

 

DC FieldValueLanguage
dc.contributor.authorZhang, Y-
dc.contributor.authorLee, CL-
dc.contributor.authorLiu, H-
dc.contributor.authorLi, X-
dc.date.accessioned2013-08-20T11:37:24Z-
dc.date.available2013-08-20T11:37:24Z-
dc.date.issued2012-
dc.identifier.citationOrganic Letters, 2012, v. 14 n. 19, p. 5146-5149-
dc.identifier.issn1523-7060-
dc.identifier.urihttp://hdl.handle.net/10722/185682-
dc.description.abstractAn efficient three-component reaction toward the facile synthesis of structurally diverse 1-carboxamido-isoindoles has been developed. The resultant isoindoles can be used in Diels-Alder reactions.-
dc.languageeng-
dc.publisherAmerican Chemical Society. The Journal's web site is located at http://pubs.acs.org/journals/orlef7/index.html-
dc.relation.ispartofOrganic Letters-
dc.subject.meshAmides - chemistry-
dc.subject.meshIsoindoles - chemical synthesis-
dc.subject.meshMolecular Structure-
dc.titleA Three-Component Reaction toward the Synthesis of 1-Carboxamido-isoindoles-
dc.typeArticle-
dc.identifier.emailLiu, H: liuhan@hku.hk-
dc.identifier.emailLi, X: xuechenl@hku.hk-
dc.identifier.authorityLiu, H=rp02748-
dc.identifier.authorityLi, X=rp00742-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ol302460s-
dc.identifier.pmid23017068-
dc.identifier.scopuseid_2-s2.0-84867386563-
dc.identifier.hkuros219114-
dc.identifier.volume14-
dc.identifier.issue19-
dc.identifier.spage5146-
dc.identifier.epage5149-
dc.identifier.isiWOS:000309438400043-
dc.publisher.placeUnited States-
dc.identifier.issnl1523-7052-

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