以手性硫催化劑進行不對稱氮丙啶化反應之研究

dc.contributor陳榮傑zh_TW
dc.contributorRong-Jie Cheinen_US
dc.contributor.author王上華zh_TW
dc.contributor.authorShang-Hua Wangen_US
dc.date.accessioned2019-09-04T09:25:54Z
dc.date.available2019-8-7
dc.date.available2019-09-04T09:25:54Z
dc.date.issued2014
dc.description.abstract以市售的5-溴基戊酸乙酯、4-正丁基溴苯或3,5-二苯基溴苯經由五步驟可得硫化物衍生物2d - 2g。我們以硫化物2d - 2g作為催化劑進行不對稱氮丙啶反應之應用,探討氫鍵催化劑對亞胺的活化作用,並成功合成出苯乙烯基氮丙啶,得到良好的產率及鏡像選擇性。zh_TW
dc.description.abstractNovel chiral tetrahydrothiophene derivatives 2b – g were synthesized from commercially available 5-bromovalerate and 4-butylbromobenzene or 3,5-diphenylbromobenzene. We demonstrate the application of these chiral sulfur catalysts in asymmetric aziridination of cinnamyl bromide and imines, and also investigate the promotion of the catalytic process by hydrogen bond catalyst such as ureas and thioureas. Vinyl-aziridines 9e - s were successfully obtained in good to excellent yields with high enantioselectivity and moderate diastereoselectivity.en_US
dc.description.sponsorship化學系zh_TW
dc.identifierGN060142031S
dc.identifier.urihttp://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=id=%22GN060142031S%22.&%22.id.&
dc.identifier.urihttp://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/100428
dc.language英文
dc.subject鋶偶極體zh_TW
dc.subject不對稱催化zh_TW
dc.subject手性zh_TW
dc.subject鏡像異構物選擇性zh_TW
dc.subject氮丙啶zh_TW
dc.subjectsulfide ylideen_US
dc.subjectasymmetric catalysisen_US
dc.subjectchiralityen_US
dc.subjectenantioselectivityen_US
dc.subjectaziridinesen_US
dc.title以手性硫催化劑進行不對稱氮丙啶化反應之研究zh_TW
dc.titleAsymmetric and Catalytic Sulfur-Ylide Mediated Aziridinationen_US

Files

Original bundle

Now showing 1 - 1 of 1
No Thumbnail Available
Name:
n060142031s01.pdf
Size:
9.74 MB
Format:
Adobe Portable Document Format

Collections