Preparation of N-aryl Aziridines
碩士 === 中原大學 === 化學研究所 === 100 === Aziridine, a high-application value compounds, not only widely used in organic synthesis reactions but also in the synthesis of natural products and medicine often have the structure of the aziridine.In recent years,many chemists put into the reserch because of the...
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ndltd-TW-100CYCU50650202015-10-13T21:32:35Z http://ndltd.ncl.edu.tw/handle/57550471258830594389 Preparation of N-aryl Aziridines 氮上有苯基取代基的氮丙啶製備 Hsin-Chi Chao 趙星智 碩士 中原大學 化學研究所 100 Aziridine, a high-application value compounds, not only widely used in organic synthesis reactions but also in the synthesis of natural products and medicine often have the structure of the aziridine.In recent years,many chemists put into the reserch because of the aziridine with the anti-tumor biological activity. In this paper, we used a series of aryl azide mix in electron- withdrawing alkenes, under high temperature and solvent environment, prepared a series of corresponding phenyl- substituted nitrogen base aziridine. The characteristics of this experiment is that without complicated steps,it can be simple and efficient to synthesis aziridine. In addition, we also try to adjust the reaction conditions, to makes the reaction selectivity better thereby allowing the production yield increase. Chia-Hsi Yang 楊嘉喜 2012 學位論文 ; thesis 131 zh-TW |
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碩士 === 中原大學 === 化學研究所 === 100 === Aziridine, a high-application value compounds, not only widely used in organic synthesis reactions but also in the synthesis of natural products and medicine often have the structure of the aziridine.In recent years,many chemists put into the reserch because of the aziridine with the anti-tumor biological activity.
In this paper, we used a series of aryl azide mix in electron- withdrawing alkenes, under high temperature and solvent environment, prepared a series of corresponding phenyl- substituted nitrogen base aziridine.
The characteristics of this experiment is that without complicated steps,it can be simple and efficient to synthesis aziridine. In addition, we also try to adjust the reaction conditions, to makes the reaction selectivity better thereby allowing the production yield increase.
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author2 |
Chia-Hsi Yang |
author_facet |
Chia-Hsi Yang Hsin-Chi Chao 趙星智 |
author |
Hsin-Chi Chao 趙星智 |
spellingShingle |
Hsin-Chi Chao 趙星智 Preparation of N-aryl Aziridines |
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Hsin-Chi Chao |
title |
Preparation of N-aryl Aziridines |
title_short |
Preparation of N-aryl Aziridines |
title_full |
Preparation of N-aryl Aziridines |
title_fullStr |
Preparation of N-aryl Aziridines |
title_full_unstemmed |
Preparation of N-aryl Aziridines |
title_sort |
preparation of n-aryl aziridines |
publishDate |
2012 |
url |
http://ndltd.ncl.edu.tw/handle/57550471258830594389 |
work_keys_str_mv |
AT hsinchichao preparationofnarylaziridines AT zhàoxīngzhì preparationofnarylaziridines AT hsinchichao dànshàngyǒuběnjīqǔdàijīdedànbǐngdìngzhìbèi AT zhàoxīngzhì dànshàngyǒuběnjīqǔdàijīdedànbǐngdìngzhìbèi |
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