Synthesis of isophthalates from methyl coumalate

dc.contributor.author Kraus, George
dc.contributor.author Wang, Shuai
dc.contributor.author Kraus, George
dc.contributor.department Chemistry
dc.date 2018-10-07T08:05:05.000
dc.date.accessioned 2020-06-30T01:16:23Z
dc.date.available 2020-06-30T01:16:23Z
dc.date.copyright Sun Jan 01 00:00:00 UTC 2017
dc.date.issued 2017-12-15
dc.description.abstract <p>Methyl coumalate reacts with enol ethers to form stable adducts which can be converted into isophthalates in good to excellent yields. Alkyl vinyl ethers afford higher yields of isophthalates than enol silyl ethers. The adduct of the enol silyl ether of acetophenone with methyl coumalate reacted with PTSA to produce a styryl coumalate.</p>
dc.description.comments <p>This article is published as Kraus, George A. and Shuai Wang. "Synthesis of isophthalates from methyl coumalate." <em>RSC Advances</em> 7, no. 89 (2017): 56760-56763. DOI: <a href="http://dx.doi.org/10.1039/C7RA12935A" target="_blank">10.1039/C7RA12935A</a>. Posted with permission.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/chem_pubs/1069/
dc.identifier.articleid 2070
dc.identifier.contextkey 12861349
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath chem_pubs/1069
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/14367
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/chem_pubs/1069/2017_Kraus_SynthesisIsophthalates.pdf|||Fri Jan 14 18:25:57 UTC 2022
dc.source.uri 10.1039/C7RA12935A
dc.subject.disciplines Environmental Chemistry
dc.subject.disciplines Organic Chemistry
dc.title Synthesis of isophthalates from methyl coumalate
dc.type article
dc.type.genre article
dspace.entity.type Publication
relation.isAuthorOfPublication 773dd84a-1494-40ee-aebf-549f26a04a22
relation.isOrgUnitOfPublication 42864f6e-7a3d-4be3-8b5a-0ae3c3830a11
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