Synthesis of novel 6-deoxyanthracyclines

dc.contributor.author Kraus, George
dc.contributor.author Hagen, Michael
dc.contributor.department Department of Chemistry
dc.date 2018-02-17T09:11:27.000
dc.date.accessioned 2020-06-30T01:22:20Z
dc.date.available 2020-06-30T01:22:20Z
dc.date.copyright Tue Jan 01 00:00:00 UTC 1985
dc.date.issued 1985-09-01
dc.description.abstract <p>An extremely direct route to the 6-deoxyanthracycline skeleton is described. The initial route to quinone 10 failed due to an unexpected complication in the Ago demethylation step. However, starting from 2-bromo- 1,4-dimethoxynaphthalene, furan 17 could be prepared in two steps. Furan 17 was then converted into anthraquinone 19 in five steps. The eight-step route proceeds in 9% overall yield.</p>
dc.description.comments <p>Reprinted (adapted) with permission from <em>The Journal of Organic Chemistry, </em>50(18); 3252-3255. Doi: <a href="http://dx.doi.org/10.1021/jo00218a002" target="_blank">10.1021/jo00218a002</a>. Copyright 1985 American Chemical Society.</p>
dc.format.mimetype application/pdf
dc.identifier archive/lib.dr.iastate.edu/chem_pubs/715/
dc.identifier.articleid 1701
dc.identifier.contextkey 7956933
dc.identifier.s3bucket isulib-bepress-aws-west
dc.identifier.submissionpath chem_pubs/715
dc.identifier.uri https://dr.lib.iastate.edu/handle/20.500.12876/15201
dc.language.iso en
dc.source.bitstream archive/lib.dr.iastate.edu/chem_pubs/715/0-1985_KrausGA_ACS_License_SynthesisNovel.pdf|||Sat Jan 15 01:43:11 UTC 2022
dc.source.bitstream archive/lib.dr.iastate.edu/chem_pubs/715/1985_KrausGA_SynthesisNovel.pdf|||Sat Jan 15 01:43:13 UTC 2022
dc.source.uri 10.1021/jo00218a002
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 Synthesis of novel 6-deoxyanthracyclines
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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