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Article: Organocatalytic mitsunobu reactions with 3,5-dinitrobenzoic acid

TitleOrganocatalytic mitsunobu reactions with 3,5-dinitrobenzoic acid
Authors
But, TYSLu, JToy, PH
Keywords(Diacetoxyiodo)Benzene
3,5-Dinitrobenzoic Acid
Catalytic Oxidation
Mitsunobu Reaction
Organocatalysis
Issue Date2010
PublisherGeorg Thieme Verlag. The Journal's web site is located at http://www.thieme-chemistry.com/thieme-chemistry/journals/info/synlett/index.shtml
Citation
Synlett, 2010 n. 7, p. 1115-1117 How to Cite?
DOI: http://dx.doi.org/10.1055/s-0029-1219795
AbstractA second generation procedure for organocatalytic Mitsunobu reactions using 3,5-dinitrobenzoic acid as the pro-nucleophile has been developed. The increased acidity of this acid compared to 4-nitrobenzoic acid, which was used in the original procedure, allowed for higher isolated yields of the desired products and eliminated formation of undesired acetate byproducts. © Georg Thieme Verlag Stuttgart - New York.
Persistent Identifierhttp://hdl.handle.net/10722/168449
ISSN
0936-5214
2021 Impact Factor: 2.170
2020 SCImago Journal Rankings: 0.712
ISI Accession Number ID
WOS:000276540500024
References
References in Scopus

 

DC FieldValueLanguage
dc.contributor.authorBut, TYSen_US
dc.contributor.authorLu, Jen_US
dc.contributor.authorToy, PHen_US
dc.date.accessioned2012-10-08T03:19:04Z-
dc.date.available2012-10-08T03:19:04Z-
dc.date.issued2010en_US
dc.identifier.citationSynlett, 2010 n. 7, p. 1115-1117en_US
dc.identifier.issn0936-5214en_US
dc.identifier.urihttp://hdl.handle.net/10722/168449-
dc.description.abstractA second generation procedure for organocatalytic Mitsunobu reactions using 3,5-dinitrobenzoic acid as the pro-nucleophile has been developed. The increased acidity of this acid compared to 4-nitrobenzoic acid, which was used in the original procedure, allowed for higher isolated yields of the desired products and eliminated formation of undesired acetate byproducts. © Georg Thieme Verlag Stuttgart - New York.en_US
dc.languageengen_US
dc.publisherGeorg Thieme Verlag. The Journal's web site is located at http://www.thieme-chemistry.com/thieme-chemistry/journals/info/synlett/index.shtmlen_US
dc.relation.ispartofSynletten_US
dc.subject(Diacetoxyiodo)Benzeneen_US
dc.subject3,5-Dinitrobenzoic Aciden_US
dc.subjectCatalytic Oxidationen_US
dc.subjectMitsunobu Reactionen_US
dc.subjectOrganocatalysisen_US
dc.titleOrganocatalytic mitsunobu reactions with 3,5-dinitrobenzoic aciden_US
dc.typeArticleen_US
dc.identifier.emailToy, PH:phtoy@hkucc.hku.hken_US
dc.identifier.authorityToy, PH=rp00791en_US
dc.description.naturelink_to_subscribed_fulltexten_US
dc.identifier.doi10.1055/s-0029-1219795en_US
dc.identifier.scopuseid_2-s2.0-77951110078en_US
dc.identifier.hkuros170477-
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-77951110078&selection=ref&src=s&origin=recordpageen_US
dc.identifier.issue7en_US
dc.identifier.spage1115en_US
dc.identifier.epage1117en_US
dc.identifier.eissn1437-2096-
dc.identifier.isiWOS:000276540500024-
dc.publisher.placeGermanyen_US
dc.identifier.scopusauthoridBut, TYS=8774303500en_US
dc.identifier.scopusauthoridLu, J=26532871800en_US
dc.identifier.scopusauthoridToy, PH=7006579247en_US
dc.identifier.issnl0936-5214-

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