利用一價銠金屬催化芳基硼酸對3號位具酯基之香豆素化合物進行不對稱1,4-加成反應

dc.contributor吳學亮zh_TW
dc.contributorWu, Hsyueh-Liangen_US
dc.contributor.author林子洋zh_TW
dc.contributor.authorLin, Zi-Yangen_US
dc.date.accessioned2020-12-14T08:58:31Z
dc.date.available2020-08-29
dc.date.available2020-12-14T08:58:31Z
dc.date.issued2020
dc.description.abstract摘要 本論文敘述利用掌性雙環 [2.2.1] 雙烯配體L5a與一價銠金屬形成之催化劑催化芳基硼酸7與三號位具酯基取代之香豆素化合物24進行不對稱1,4-加成反應。此加成反應產生9−99%產率,鏡像超越值7−99%的加成產物25。此方法可以用於合成抗利尿藥物 (R)–Tolterodine (14)zh_TW
dc.description.abstractAbstract This thesis describes an asymmetric 1,4-conjugated addition reaction of arylboronic acids 7 to various coumarin-3-carboxylic esters 24 in the presence of 3.0 mol % Rh(Ⅰ)-catalyst consisting of chiral diene ligand L5a, affording adducts 25 in up to 99% yield, d.r > 20:1 and 99% ee. This asymmetric transformation demonstrates its usefulness in the synthesis of an anti-diuretic drug, (R)–Tolterodine (14)en_US
dc.description.sponsorship化學系zh_TW
dc.identifierG060742039S
dc.identifier.urihttp://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=id=%22G060742039S%22.&
dc.identifier.urihttp://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/111147
dc.language中文
dc.subject銠金屬催化zh_TW
dc.subject掌性雙烯配基zh_TW
dc.subject1zh_TW
dc.subject4-加成反應zh_TW
dc.subjectRh(Ⅰ)-catalysten_US
dc.subjectchiral diene liganden_US
dc.subject1en_US
dc.subject4-addition reactionen_US
dc.title利用一價銠金屬催化芳基硼酸對3號位具酯基之香豆素化合物進行不對稱1,4-加成反應zh_TW
dc.titleEnantioselective 1,4-Arylation of Coumarin-3-carboxylic Esters Using Rh(І)/Diene Catalystsen_US

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