A Dissertation Presented to the Faculty of the Graduate School of Arts and Sciences of Braitdeis University, Waltham , Massachusetts

dc.contributor.advisorStevenson, Robert (Professor)
dc.contributor.authorBiftu, Tesfaye
dc.date.accessioned2018-07-19T09:30:02Z
dc.date.accessioned2023-11-09T16:18:20Z
dc.date.available2018-07-19T09:30:02Z
dc.date.available2023-11-09T16:18:20Z
dc.date.issued1978-08
dc.description.abstract2,3- Diaroylbutanes were selectively converted with high stereospecificity to 2,5~diaryl“3,4-dimethylfurans or 2,3- diarylbutanes. The racemic forms of the dibenzylbutane lignans, dihydroguaiaretic acid dimethyl ether 26a, austrobilignan- 5 26b and austrobilignan-6 26 e * and the diaryltetrahydrofuran lignans, veraguensin 27a and its piperonyl analogue 27 b have been readily synthesized. The synthesis of the dissimilar substituted 2^"diaryltetrahydrofuran austrobilignan- 7 27er was limited by isomer formation and separation difficulty. A short convenient synthesis of the aryltetralin lignan, galbulin 37a and the all-trans tetrahydrofuran lignan, / galbelgiri 31a are also reported. 1,4- Diarylbutanes undergo yield dibenzo [a,c] cyclooctenes. Short synthetic routes to the lignan , (+ )-deoxyschizandrin 43d have been developed from 3,4, 5-trimethoxypropiophenone.en_US
dc.identifier.urihttp://etd.aau.edu.et/handle/12345678/9447
dc.language.isoenen_US
dc.publisherAddis Ababa Universtyen_US
dc.subjectArts and Sciencesen_US
dc.titleA Dissertation Presented to the Faculty of the Graduate School of Arts and Sciences of Braitdeis University, Waltham , Massachusettsen_US
dc.typeThesisen_US

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