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Stereoselective Total Syntheses of Musellarins D and E
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.advisor | 이동주 | - |
| dc.contributor.author | 한재혁 | - |
| dc.date.accessioned | 2025-01-25T01:36:11Z | - |
| dc.date.available | 2025-01-25T01:36:11Z | - |
| dc.date.issued | 2023-02 | - |
| dc.identifier.other | 32797 | - |
| dc.identifier.uri | https://dspace.ajou.ac.kr/handle/2018.oak/24705 | - |
| dc.description | 학위논문(석사)--아주대학교 일반대학원 :약학과,2023. 2 | - |
| dc.description.tableofcontents | I. Introduction 1 <br>II. Results and Discussion 3 <br>III. Conclusion 8 <br>IV. Experimental Section 9 <br> 1. Materials and Methods 9 <br> 2. Full Experimental Procedures and Analytical Data of Compounds 11 <br>V. References 27 <br>VI. Appendix 29 | - |
| dc.language.iso | eng | - |
| dc.publisher | The Graduate School, Ajou University | - |
| dc.rights | 아주대학교 논문은 저작권에 의해 보호받습니다. | - |
| dc.title | Stereoselective Total Syntheses of Musellarins D and E | - |
| dc.type | Thesis | - |
| dc.contributor.affiliation | 아주대학교 대학원 | - |
| dc.contributor.alternativeName | Jae-hyuk Han | - |
| dc.contributor.department | 일반대학원 약학과 | - |
| dc.date.awarded | 2023-02 | - |
| dc.description.degree | Master | - |
| dc.identifier.localId | T000000032797 | - |
| dc.identifier.url | https://dcoll.ajou.ac.kr/dcollection/common/orgView/000000032797 | - |
| dc.subject.keyword | Dehydrogenative Cycloetherification | - |
| dc.subject.keyword | Diastereoselectivity | - |
| dc.subject.keyword | Musellarins D and E | - |
| dc.subject.keyword | Natural Products | - |
| dc.subject.keyword | cis-2-Alkyl-6-aryl-3 | - |
| dc.subject.keyword | 6-dihydro-2H-pyran | - |
| dc.description.alternativeAbstract | The first and unified stereoselective total syntheses of naturally occurring (+)-musellarin D and musellarin E have been accomplished in 8 steps from the readily available α-tetralone, respectively. The key feature of our strategy includes highly diastereoselective dehydrogenative etherification and substrate-controlled benzylic allylation. The relative configuration of both musellarins D and E was revised. | - |
- Appears in Collections:
- Graduate School of Ajou University > Department of Pharmacy > 3. Theses(Master)
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