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A synthesis of (+)-7-Epiaustraline and (-)-7-Epialexine

dc.contributor.authorPearson, William H.en_US
dc.contributor.authorHines, Jennifer V.en_US
dc.date.accessioned2006-04-10T14:34:55Z
dc.date.available2006-04-10T14:34:55Z
dc.date.issued1991-09-30en_US
dc.identifier.citationPearson,, William H., Hines, Jennifer V. (1991/09/30)."A synthesis of (+)-7-Epiaustraline and (-)-7-Epialexine." Tetrahedron Letters 32(40): 5513-5516. <http://hdl.handle.net/2027.42/29124>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6THS-42K69PH-P/2/b0613875b8fd57ecb7a66eb5635eab1een_US
dc.identifier.urihttps://hdl.handle.net/2027.42/29124
dc.description.abstractReductive cyclization of the azido epoxides 19[alpha] and 19[beta] followed by deprotection afforded the HIV inhibitor (+)-7-epiaustraline 7 and (-)-7-epialexine 9. The formation of 7 proceeded with an unusual inversion of configuration at C-7.en_US
dc.format.extent339607 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleA synthesis of (+)-7-Epiaustraline and (-)-7-Epialexineen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMaterials Science and Engineeringen_US
dc.subject.hlbsecondlevelChemistryen_US
dc.subject.hlbsecondlevelChemical Engineeringen_US
dc.subject.hlbsecondlevelBiological Chemistryen_US
dc.subject.hlbtoplevelEngineeringen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry, The University of Michigan, Ann Arbor, MI 48109-1055 U.S.A.en_US
dc.contributor.affiliationumDepartment of Medicinal Chemistry, The University of Michigan, Ann Arbor, MI 48109-1055 U.S.A.en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/29124/1/0000163.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0040-4039(91)80071-Den_US
dc.identifier.sourceTetrahedron Lettersen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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