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Lewis Acid-Promoted Diastereoselective Construction of Arylated Quaternary Stereogenic Centers
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dc.contributor.advisorDongjoo Lee-
dc.contributor.author손희주-
dc.date.issued2024-02-
dc.identifier.other33789-
dc.identifier.urihttps://aurora.ajou.ac.kr/handle/2018.oak/39143-
dc.description학위논문(석사)--약학과,2024. 2-
dc.description.abstractWe report a strategy for forming an arylated quaternary carbon center based on an allylation reaction to form a quaternary stereogenic center stereoselectively. The primary strategy involves introducing Allyl via Lewis Acid into Diol, a readily accessible compound, to generate a Quaternary Carbon center. This strategy is a reasonable synthetic method for efficiently constructing a quaternary stereogenic center in tertiary alcohol, where the introduction of substituents is difficult due to steric hindrance.-
dc.description.tableofcontentsI. Introduction 1_x000D_ <br>II. Results and Discussion 3_x000D_ <br>III. Conclusion 11_x000D_ <br>IV. Experimental Section 12_x000D_ <br>1. Materials and Methods 12_x000D_ <br>2. Full Experimental Procedures and Analytical Data of Compounds 14_x000D_ <br>V. References 55_x000D_ <br>VI. Appendix 57-
dc.language.isoeng-
dc.publisherThe Graduate School, Ajou University-
dc.rights아주대학교 논문은 저작권에 의해 보호받습니다.-
dc.titleLewis Acid-Promoted Diastereoselective Construction of Arylated Quaternary Stereogenic Centers-
dc.typeThesis-
dc.contributor.affiliation아주대학교 대학원-
dc.contributor.alternativeNameSON HEE JU-
dc.contributor.department일반대학원 약학과-
dc.date.awarded2024-02-
dc.description.degreeMaster-
dc.identifier.urlhttps://dcoll.ajou.ac.kr/dcollection/common/orgView/000000033789-
dc.subject.keywordAllylation-
dc.subject.keywordArylated Quaternary Stereogenic Center-
dc.subject.keywordDiastereoselectivity-
dc.subject.keywordLewis Acid-
dc.subject.keywordMesemebrane-
dc.subject.keywordNatural Products-
dc.subject.keywordTertiary Alcohol-
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