Please use this identifier to cite or link to this item: http://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/100982
Full metadata record
DC FieldValueLanguage
dc.contributor簡敦誠zh_TW
dc.contributorChien, Tun-Chengen_US
dc.contributor.author鍾元棟zh_TW
dc.contributor.authorJhong, Yuan-dongen_US
dc.date.accessioned2019-09-04T10:18:26Z-
dc.date.available2022-07-31
dc.date.available2019-09-04T10:18:26Z-
dc.date.issued2012
dc.identifierGN0699420871
dc.identifier.urihttp://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=%22http://etds.lib.ntnu.edu.tw/cgi-bin/gs32/gsweb.cgi?o=dstdcdr&s=id=%22GN0699420871%22.&%22.id.&
dc.identifier.urihttp://rportal.lib.ntnu.edu.tw:80/handle/20.500.12235/100982-
dc.description.abstract  本篇論文主要分為兩個部份。第一部份主旨為 GFP 吸光基團類似物的合成研究。利用 N-acylglycine 為起始物,在醋酸鈉 / 醋酸酐的條件下與各種取代基的苯甲醛進行 Erlenmeyer azlactone synthesis 反應形成 4-arylidene-5-oxazolinone 衍生物。接下來再使用一級胺在室溫下對 oxazolinone 進行開環反應,可以得到含有直鏈結構的 N-alkyl-2-acylamido-3-arylacrylamide。接下來有兩個方法可以進行合環反應,一個是使用 pyridine 作為反應試劑和反應溶劑,進行脫水合環反應形成 4-arylidene-5-imidazolinone 衍生物,適用於不同官能基上;另外一個是使用改良後的 Mitsunobu 反應,一樣可以進行合環反應,雖然有些例子產率不高,但這是一個較為溫和的反應。   第二部份是合成 α-(pyrrol-2-yl)pyrrolidine 衍生物。使用氮上有 Bn 保護的 proline 當作起始物,與 thionyl chloride 反應得到醯氯的中間物,隨後使用鹼和 pyrrole 反應,得到α-(pyrrol-2-yl)pyrrolidine 衍生物。在本論文中,我們研究了本反應的適用性,並用來製備一系列α-(pyrrol-2-yl)pyrrolidine 衍生物。zh_TW
dc.description.abstractThis thesis is divided into two parts. The main focus of the first part is to study the synthesis of Green Fluorescent Protein (GFP) chromophore analogs. N-acylglycine as the starting material was heated with sodium acetate and various benzaldehydes in acetic anhydride to undergo the Erlenmeyer azlactone synthesis reaction to afford a series of 4-arylidene-5-oxazolinones. The oxazolinones were treated with primary amines to give the ring-opened adducts which contain the N-alkyl-2-acylamido-3-arylacrylamide moiety. We first demonstrated that, using pyridine as the reagent and solvent, the ring-opened adducts were heated in pyridine to undergo the dehydrative cyclization reaction to afford the ring-closed 4-arylidene-5-imidazolinone derivatives as the GFP chromophore analogs. Alternatively, our investigation also showed that a modified Mitsunobu reaction condition could also accomplish the same reaction to give the 4-arylidene-5-imidazolinone derivatives.   The second part reported a novel reaction for the synthesis of α-(pyrrol-2-yl)pyrrolidine derivatives. N-benzylproline as starting material was treated with thionyl chloride to afford the acyl chloride intermediate. Subsequently, pyrrole was added in the presence of a base to result a decarbonylated product which was identified as an α-(pyrrol-2-yl)pyrrolidine derivative. The scope and generality were examined and the reaction is applicable to a series of pyrrole derivatives.en_US
dc.description.sponsorship化學系zh_TW
dc.language中文
dc.subjectProlinezh_TW
dc.subjectPyrrolezh_TW
dc.subject脫羧基耦合zh_TW
dc.subjectprolineen_US
dc.subjectpyrroleen_US
dc.subjectdecarboxylative couplingen_US
dc.title經由 Proline 及 Pyrrole 進行脫羧基耦合反應製備 2-(Pyrrol-2-yl)pyrrolidinezh_TW
dc.titleStudy on the synthesis of 2-(pyrrol-2-yl)pyrrolidines from the decarboxylative coupling of proline and pyrroleen_US
Appears in Collections:學位論文

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.