Please use this identifier to cite or link to this item: http://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/111155
Title: 利用一價銠金屬進行不對稱1,4-加成反應對三尖杉鹼天然物全合成之合成研究
A Synthetic Study Toward the Total Synthesis of (−)-Cephalotaxine Using Rh(I)-Catalyzed Enantioselective 1,4-Addition Reaction
Authors: 吳學亮
Wu, Hsyueh-Liang
呂怡柔
Lu, Yi-Rou
Keywords: 一價銠金屬
掌性雙環[2.2.1]雙烯配基
環狀α,β-不飽和β-酮酯
不對稱1,4-加成反應
天然物
Rh(I)/chiral diene ligand catalyst
asymmetric 1,4-addition reaction
α,β-unsaturated β-ketoester
natural product
Issue Date: 2020
Abstract: 本篇論文探討利用一價銠金屬及掌性雙環[2.2.1]雙烯配基L1形成之催化劑催化芳香基硼酸試劑48對環狀α,β-不飽和β-酮酯47進行不對稱1,4-加成反應。生成加成產物46為單一非鏡像異構物有產率67–99%及鏡像超越值66–99%。此加成產物46可再進行烷基化反應(C-alkylation),建構掌性四級碳之產物45,其產物45產率43–94%及鏡像超越值66–98%。本論文探討利用此方法應用在合成天然物(−)-Cephalotaxine之可能性
This thesis studies the asymmetric 1,4-addition reaction of arylboronic acids 48 to cyclic α,β-unsaturated β-ketoester 47 catalyzed by a Rh(I)/chiral diene ligand L1 catalyst. The adducts 46 were obtained as a single diastereomer in up to 99% yield and with up to 99% ee. Furthermore, the adducts 46 underwent C-alkylaion reaction to provide products 45 with a chiral quaternary stereogenic center in up to 94% yield and with up to 98% ee. This method was used for the synthetic study toward the total synthesis of natural product (−)-Cephalotaxine.
URI: http://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=id=%22G060742051S%22.&%22.id.&
http://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/111155
Other Identifiers: G060742051S
Appears in Collections:學位論文

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