博碩士論文 102223035 完整後設資料紀錄

DC 欄位 語言
DC.contributor化學學系zh_TW
DC.creator鍾政宇zh_TW
DC.creatorCheng-Yu Chungen_US
dc.date.accessioned2016-1-8T07:39:07Z
dc.date.available2016-1-8T07:39:07Z
dc.date.issued2016
dc.identifier.urihttp://ir.lib.ncu.edu.tw:88/thesis/view_etd.asp?URN=102223035
dc.contributor.department化學學系zh_TW
DC.description國立中央大學zh_TW
DC.descriptionNational Central Universityen_US
dc.description.abstract本篇研究是以D-Ribose作為起始物合成目標天然物(+)-Pericosine A, (-)-Pericosine C和(+)-Pericosine E。主要的反應有Wittig反應和Swern氧化反應。以[α-(Alkoxycarbonyl)vinyl]aluminium作為具有非鏡像選擇性的羰基加成反應可得到重要的中間產物8a和8b。(+)-Pericosine A可在化合物8a進行環合置換(Ring-Closing Metathesis)反應後,參考Stevenson教授的合成方法而得。化合物8a經由環合置換反應合環、鈀催化的allylic substitution後可得到(-)-Pericosine C。(+)-Pericosine E應亦可藉由鈀催化的allylic substitution而得,然而尚在進行中。zh_TW
dc.description.abstractSuccessfully synthesizing natural product (+)-Pericosine A, (-)-Periciosine C,(+)-Pericosine E was the aim. The main reactions we used are Wittig reaction, Swern oxidation, [α-(Alkoxycarbonyl)-vinyl]aluminum reaction and Palladium-catalyzed allylic substitution. Diastereomeric intermediate 8a and 8b can be synthesized via [α-(Alkoxycarbonyl)-vinyl]aluminum reaction which the ratio is 4 to 1. (+)-Pericosine A was obtained by compound 8a through Ring-Closing metathesis then directly referring to Prof. Stevenson’s method. (-)-Pericosine C was obtained by compound 8a via Ring-Closing Metathesis and Palladium-catalyzed allylic substitution successfully. (+)-Pericosine E might can be synthesized by Palladium-catalyzed allylic substitution, but still doing effort right now.en_US
DC.subject非鏡像選擇性zh_TW
DC.subject鈀催化zh_TW
DC.subject[α-(Alkoxycarbonyl)vinyl]aluminium reactionen_US
DC.subjectallylic substitutionen_US
DC.title天然物(+)-Pericosine A, (-)-Pericosine C, (+)-Pericosine E的合成研究zh_TW
dc.language.isozh-TWzh-TW
DC.type博碩士論文zh_TW
DC.typethesisen_US
DC.publisherNational Central Universityen_US

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