Stereoselective Total Syntheses of Musellarins D and E

Author(s)
한재혁
Alternative Author(s)
Jae-hyuk Han
Advisor
이동주
Department
일반대학원 약학과
Publisher
The Graduate School, Ajou University
Publication Year
2023-02
Language
eng
Keyword
Dehydrogenative CycloetherificationDiastereoselectivityMusellarins D and ENatural Productscis-2-Alkyl-6-aryl-36-dihydro-2H-pyran
Alternative Abstract
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.
URI
https://dspace.ajou.ac.kr/handle/2018.oak/24705
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Graduate School of Ajou University > Department of Pharmacy > 3. Theses(Master)
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