Synthesis of Flinderole Derivatives

dc.contributorMay, Jeremy A.
dc.contributor.authorSales, Karlo K.
dc.contributor.authorVallakati, Ravikrishna
dc.date.accessioned2018-02-27T15:56:56Z
dc.date.available2018-02-27T15:56:56Z
dc.date.issued2017-10-12
dc.description.abstractA three-step synthesis of tryptamine to flindersial alkaloids has as its last step an acid promoted dimerization to borrerine, a related natural product. Methylation with dimethyl sulfate in the last step followed by dimerization forms Flinderole B, C and Dimethylisoborreverine.
dc.description.departmentChemistry, Department of
dc.description.departmentHonors College
dc.identifier.urihttp://hdl.handle.net/10657/2567
dc.language.isoen_US
dc.rightsThe author of this work is the copyright owner. UH Libraries and the Texas Digital Library have their permission to store and provide access to this work. Further transmission, reproduction, or presentation of this work is prohibited except with permission of the author(s).
dc.titleSynthesis of Flinderole Derivatives
dc.typePoster

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