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Total Synthesis of an Antifouling Marine Furanosesquiterpene

dc.contributor.authorUngarean, Chad N.
dc.contributor.authorMason, Jeremy D.
dc.contributor.authorEyer, Benjamin R.
dc.contributor.authorDuca, Nicholas S.
dc.contributor.authorMong, Jaimie M.
dc.contributor.authorMurphree, S. Shaun
dc.date.accessioned2017-07-17T13:44:22Z
dc.date.available2017-07-17T13:44:22Z
dc.date.issued2017-02-10
dc.identifier.citationUngarean, C.N., et al. (2017). Total Synthesis of an Antifouling Marine Furanosesquiterpene. Synthesis 49(10): 2177-2181. doi: 10.1055/s-0036-1588711.en_US
dc.identifier.issn0039-7881
dc.identifier.issne1437-210X
dc.identifier.urihttp://hdl.handle.net/10456/44791
dc.description.abstractAn antifouling sesquiterpene isolated from Sinularia sp. was synthesized from citronellyl acetate in eight steps and 9% overall yield. The furan moiety was constructed using a multifunctional sulfone reagent.en_US
dc.description.sponsorshipPetroleum Research Fund (PRF 42382-B1) / Arnold and Mabel Beckman Foundation / Shanbrom Fund of Allegheny Collegeen_US
dc.language.isoen_USen_US
dc.publisherThiemeen_US
dc.relation.ispartofSynthesisen_US
dc.relation.isversionofhttps://www.thieme-connect.com/products/ejournals/html/10.1055/s-0036-1588711en_US
dc.rightsPublisher's version can be used on author's personal website only. Post print can be used in a repository after a 12 month embargo.en_US
dc.subjectfuransen_US
dc.subjectsulfonesen_US
dc.subjectnatural productsen_US
dc.subjecttotal synthesisen_US
dc.subjectheterocyclesen_US
dc.titleTotal Synthesis of an Antifouling Marine Furanosesquiterpeneen_US
dc.description.versionPublished articleen_US
dc.contributor.departmentChemistryen_US
dc.description.embargoPost print of this article will be made available to the public after February 10, 2018.en_US
dc.citation.volume49en_US
dc.citation.issue10en_US
dc.citation.spage2177en_US
dc.citation.epage2181en_US
dc.identifier.doi10.1055/s-0036-1588711
dc.contributor.avlauthorMurphree, S. Shaun


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