A direct synthesis of c-glycosyl compounds

dc.contributor.author Kraus, George
dc.contributor.author Molina, Maria
dc.contributor.department Department of Chemistry
dc.date 2018-02-17T09:06:14.000
dc.date.accessioned 2020-06-30T01:22:00Z
dc.date.available 2020-06-30T01:22:00Z
dc.date.copyright Fri Jan 01 00:00:00 UTC 1988
dc.date.issued 1988-02-01
dc.description.abstract <p>Lactone 4 (R = Bn) can be converted into C-glycosyl compounds by reaction with an organometallic reagent followed by reduction with Et,SiH and BF3.Et20.</p>
dc.description.comments <p>Reprinted (adapted) with permission from <em>The Journal of Organic Chemistry, </em>53(4); 752-753. Doi: <a href="http://dx.doi.org/10.1021/jo00239a009" target="_blank">10.1021/jo00239a009</a>. Copyright 1988 American Chemical Society.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/chem_pubs/678/
dc.identifier.articleid 1678
dc.identifier.contextkey 7954360
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath chem_pubs/678
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/15159
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/chem_pubs/678/0-1988_KrausGA_ACS_License_DirectSynthesisCGlycosides.pdf|||Sat Jan 15 01:28:10 UTC 2022
dc.source.bitstream archive/lib.dr.iastate.edu/chem_pubs/678/1988_KrausGA_DirectSynthesisCGlycosides.pdf|||Sat Jan 15 01:28:12 UTC 2022
dc.source.uri 10.1021/jo00239a009
dc.subject.disciplines Chemistry
dc.subject.disciplines Environmental Chemistry
dc.subject.disciplines Inorganic Chemistry
dc.subject.disciplines Organic Chemistry
dc.subject.disciplines Other Chemistry
dc.subject.disciplines Polymer Chemistry
dc.title A direct synthesis of c-glycosyl compounds
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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