Highly Enantioselective Synthesis of Cyclopentane from Newly Developed Coumarin Derivatives by Organocatalytic Asymmetric (3+2) Cyclization

碩士 === 國立臺灣師範大學 === 化學系 === 105 === Coumarin derivatives have the large biological activity, and in nature are also important natural product, therefore, how to make the addition on coumarin derivatives becomes a very important issue. In the past, we mostly construct five heteroatomed ring on the c...

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Main Authors: Chen, Kai-Han, 陳楷涵
Other Authors: Lin, Wen-Wei
Format: Others
Language:zh-TW
Published: 2017
Online Access:http://ndltd.ncl.edu.tw/handle/kefd2q
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spelling ndltd-TW-105NTNU50650592019-05-15T23:46:59Z http://ndltd.ncl.edu.tw/handle/kefd2q Highly Enantioselective Synthesis of Cyclopentane from Newly Developed Coumarin Derivatives by Organocatalytic Asymmetric (3+2) Cyclization 利用新開發的香豆素衍生物經由 (3+2) 合環合成具有高鏡像選擇性的五碳環化合物 Chen, Kai-Han 陳楷涵 碩士 國立臺灣師範大學 化學系 105 Coumarin derivatives have the large biological activity, and in nature are also important natural product, therefore, how to make the addition on coumarin derivatives becomes a very important issue. In the past, we mostly construct five heteroatomed ring on the coumarin in asymmetric-organocatalyzed reaction. Nowadays, we use the newly developed coumarin derivatives as the substrates, and develope the great strategy to establish the five-carbon ring on the coumarin derivatives, and use the intermediates to figure out this reaction mechanism. In the second part, the synthesis of complex compounds in organic reactions usually requires the construction of the steps via the multi-step reaction step. However, due to the fact that the multi-step reaction is liable to the waste of resources, so research has become an important subject through the domimo reaction. This part focusing on the development of serial reaction initiation ideas and test results. Lin, Wen-Wei 林文偉 2017 學位論文 ; thesis 315 zh-TW
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language zh-TW
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description 碩士 === 國立臺灣師範大學 === 化學系 === 105 === Coumarin derivatives have the large biological activity, and in nature are also important natural product, therefore, how to make the addition on coumarin derivatives becomes a very important issue. In the past, we mostly construct five heteroatomed ring on the coumarin in asymmetric-organocatalyzed reaction. Nowadays, we use the newly developed coumarin derivatives as the substrates, and develope the great strategy to establish the five-carbon ring on the coumarin derivatives, and use the intermediates to figure out this reaction mechanism. In the second part, the synthesis of complex compounds in organic reactions usually requires the construction of the steps via the multi-step reaction step. However, due to the fact that the multi-step reaction is liable to the waste of resources, so research has become an important subject through the domimo reaction. This part focusing on the development of serial reaction initiation ideas and test results.
author2 Lin, Wen-Wei
author_facet Lin, Wen-Wei
Chen, Kai-Han
陳楷涵
author Chen, Kai-Han
陳楷涵
spellingShingle Chen, Kai-Han
陳楷涵
Highly Enantioselective Synthesis of Cyclopentane from Newly Developed Coumarin Derivatives by Organocatalytic Asymmetric (3+2) Cyclization
author_sort Chen, Kai-Han
title Highly Enantioselective Synthesis of Cyclopentane from Newly Developed Coumarin Derivatives by Organocatalytic Asymmetric (3+2) Cyclization
title_short Highly Enantioselective Synthesis of Cyclopentane from Newly Developed Coumarin Derivatives by Organocatalytic Asymmetric (3+2) Cyclization
title_full Highly Enantioselective Synthesis of Cyclopentane from Newly Developed Coumarin Derivatives by Organocatalytic Asymmetric (3+2) Cyclization
title_fullStr Highly Enantioselective Synthesis of Cyclopentane from Newly Developed Coumarin Derivatives by Organocatalytic Asymmetric (3+2) Cyclization
title_full_unstemmed Highly Enantioselective Synthesis of Cyclopentane from Newly Developed Coumarin Derivatives by Organocatalytic Asymmetric (3+2) Cyclization
title_sort highly enantioselective synthesis of cyclopentane from newly developed coumarin derivatives by organocatalytic asymmetric (3+2) cyclization
publishDate 2017
url http://ndltd.ncl.edu.tw/handle/kefd2q
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