(I) Synthesis of benzimidazole linked indoline derivative by acid catalyst(II) One-pot synthesis of derivative of ellipticine which has the activity against Mycobacterium tuberculosis

碩士 === 國立交通大學 === 應用化學系碩博士班 === 105 === This thesis has two parts: The first part is about synthesis of benzimidazole linked indoline derivatives from C-2-linked-o-aminobenzyl benzimidazole by acid catalyst. This method can apply to various funtional groups. There is no published paper refer to benz...

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Main Authors: Chiu, Feng-Yu, 邱夆昱
Other Authors: Sun, Chung-Min
Format: Others
Language:zh-TW
Published: 2017
Online Access:http://ndltd.ncl.edu.tw/handle/3snnw5
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spelling ndltd-TW-105NCTU55000672019-05-16T00:08:11Z http://ndltd.ncl.edu.tw/handle/3snnw5 (I) Synthesis of benzimidazole linked indoline derivative by acid catalyst(II) One-pot synthesis of derivative of ellipticine which has the activity against Mycobacterium tuberculosis (I) 酸催化合成苯并咪唑連接吲哚啉衍生物(II) 一鍋化合成具有抗結核菌活性之橢圓玫瑰樹鹼衍生物 Chiu, Feng-Yu 邱夆昱 碩士 國立交通大學 應用化學系碩博士班 105 This thesis has two parts: The first part is about synthesis of benzimidazole linked indoline derivatives from C-2-linked-o-aminobenzyl benzimidazole by acid catalyst. This method can apply to various funtional groups. There is no published paper refer to benzimidazole linked indoline derivatives, so we hope these heterobicyclic molecules can show more bioactivity and also hope this thesis can open a new page for research of drugs. The second part is about One-pot synthesis of derivative of ellipticine which has the activity against Mycobacterium tuberculosis. We hope we can improve its activity of anti-TB by changing different funtional groups to study the structure–activity relationship. Sun, Chung-Min 孫仲銘 2017 學位論文 ; thesis 47 zh-TW
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language zh-TW
format Others
sources NDLTD
description 碩士 === 國立交通大學 === 應用化學系碩博士班 === 105 === This thesis has two parts: The first part is about synthesis of benzimidazole linked indoline derivatives from C-2-linked-o-aminobenzyl benzimidazole by acid catalyst. This method can apply to various funtional groups. There is no published paper refer to benzimidazole linked indoline derivatives, so we hope these heterobicyclic molecules can show more bioactivity and also hope this thesis can open a new page for research of drugs. The second part is about One-pot synthesis of derivative of ellipticine which has the activity against Mycobacterium tuberculosis. We hope we can improve its activity of anti-TB by changing different funtional groups to study the structure–activity relationship.
author2 Sun, Chung-Min
author_facet Sun, Chung-Min
Chiu, Feng-Yu
邱夆昱
author Chiu, Feng-Yu
邱夆昱
spellingShingle Chiu, Feng-Yu
邱夆昱
(I) Synthesis of benzimidazole linked indoline derivative by acid catalyst(II) One-pot synthesis of derivative of ellipticine which has the activity against Mycobacterium tuberculosis
author_sort Chiu, Feng-Yu
title (I) Synthesis of benzimidazole linked indoline derivative by acid catalyst(II) One-pot synthesis of derivative of ellipticine which has the activity against Mycobacterium tuberculosis
title_short (I) Synthesis of benzimidazole linked indoline derivative by acid catalyst(II) One-pot synthesis of derivative of ellipticine which has the activity against Mycobacterium tuberculosis
title_full (I) Synthesis of benzimidazole linked indoline derivative by acid catalyst(II) One-pot synthesis of derivative of ellipticine which has the activity against Mycobacterium tuberculosis
title_fullStr (I) Synthesis of benzimidazole linked indoline derivative by acid catalyst(II) One-pot synthesis of derivative of ellipticine which has the activity against Mycobacterium tuberculosis
title_full_unstemmed (I) Synthesis of benzimidazole linked indoline derivative by acid catalyst(II) One-pot synthesis of derivative of ellipticine which has the activity against Mycobacterium tuberculosis
title_sort (i) synthesis of benzimidazole linked indoline derivative by acid catalyst(ii) one-pot synthesis of derivative of ellipticine which has the activity against mycobacterium tuberculosis
publishDate 2017
url http://ndltd.ncl.edu.tw/handle/3snnw5
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