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Concise syntheses of notoamides B-E and stephacidin A

dc.contributor.authorGrubbs, Alan Whitfield, author
dc.date.accessioned2024-03-13T19:53:49Z
dc.date.available2024-03-13T19:53:49Z
dc.date.issued2008
dc.description.abstractPresented herein are concise syntheses of the cytotoxic alkaloids notoamides B-E. A highly convergent synthesis is outlined from commercially available 6-hydroxy indole and naturally derived L(-)-Proline or L(-)-cis-3-hydroxy Proline. Also presented is a 16 step synthesis of (±)-11-epi -norgeamide B and finally a concise 17 step synthesis of stephacidin A. The synthesis of each member of the norgeamide and notoamide family of natural products is proposed via the tunable activation or deactivation of the 1,7-dihydropyrano[2,3-g]indole ring system in order to exploit a mild Pinacol-type rearrangement en-route to notoamides A-C and norgeamides A and B, or the prevention thereof, to allow access to the pyrroloindole scaffold of norgeamides C and D or notoamide D.
dc.format.mediumborn digital
dc.format.mediumdoctoral dissertations
dc.identifierETDF_Grubbs_2008_3332714.pdf
dc.identifier.urihttps://hdl.handle.net/10217/237765
dc.languageEnglish
dc.language.isoeng
dc.publisherColorado State University. Libraries
dc.relation.ispartof2000-2019
dc.rightsCopyright and other restrictions may apply. User is responsible for compliance with all applicable laws. For information about copyright law, please see https://libguides.colostate.edu/copyright.
dc.rights.licensePer the terms of a contractual agreement, all use of this item is limited to the non-commercial use of Colorado State University and its authorized users.
dc.subjectmarcfortine
dc.subjectnatural products
dc.subjectnorgeamide
dc.subjectnotoamides
dc.subjectstephacidin
dc.subjectorganic chemistry
dc.subjectpharmaceutical sciences
dc.titleConcise syntheses of notoamides B-E and stephacidin A
dc.typeText
dcterms.rights.dplaThis Item is protected by copyright and/or related rights (https://rightsstatements.org/vocab/InC/1.0/). You are free to use this Item in any way that is permitted by the copyright and related rights legislation that applies to your use. For other uses you need to obtain permission from the rights-holder(s).
thesis.degree.disciplineChemistry
thesis.degree.grantorColorado State University
thesis.degree.levelDoctoral
thesis.degree.nameDoctor of Philosophy (Ph.D.)

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