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dc.contributorWichita State University. Department of Chemistryen_US
dc.contributor.authorMeece, Frederick A.en_US
dc.contributor.authorJayasinghe, Champika P.en_US
dc.contributor.authorHistand, Garyen_US
dc.contributor.authorBurns, Dennis H.en_US
dc.date.accessioned2012-02-06T17:17:05Z
dc.date.available2012-02-06T17:17:05Z
dc.date.issued2009-04-17en_US
dc.identifier19284780en_US
dc.identifier2985193Ren_US
dc.identifier.citationThe Journal of organic chemistry. 2009 Apr 17; 74(8): 3156-9.en_US
dc.identifier.issn1520-6904en_US
dc.identifier.issn0022-3263en_US
dc.identifier.urihttp://dx.doi.org/10.1021/jo900002nen_US
dc.identifier.urihttp://hdl.handle.net/10057/4391
dc.descriptionClick on the DOI link below to access the article (may not be free).en_US
dc.description.abstractA method for the one-step C-ureidoalkylation of phenol, anisole, or aniline rings furnishing ArCH(2)NHCONHR (Ar = benzyl) products in moderate to good yields is described. With phenol ring systems, higher yields were attained when the reaction was worked up with an acidic ethanethiol addition to cleave any O-ureidoalkylation products that formed during the reaction.en_US
dc.format.extent3156-9en_US
dc.language.isoengen_US
dc.publisherAmerican Chemical Societyen_US
dc.relation.ispartofseriesThe Journal of organic chemistryen_US
dc.relation.ispartofseriesJ. Org. Chem.en_US
dc.sourceNLMen_US
dc.titleA convenient, one-step synthesis of benzyl (Ar) ureas of the type ArCH(2)NHCONHR from Ar and R(1)OCH(2)NHCONHR via ureidoalkylationen_US
dc.typeArticleen_US
dc.coverage.spacialUnited Statesen_US
dc.description.versionpeer revieweden_US
dc.rights.holderCopyright © 2009 American Chemical Societyen_US


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