Synthetic Studies on the Key Intermediate of Potent Anti-tumor Natural Products-Saframycin A

碩士 === 朝陽科技大學 === 應用化學系碩士班 === 91 === Saframycin A (1a) is one kind of natural products which show potent antitumor antibiotics. Due to the scant availability from natural sources and difficulty in cultivation, we make an attempt to synthsize derivatives of the Saframycin A (1a) by means of organic...

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Main Authors: Meng-Tsung Li, 李孟宗
Other Authors: none
Format: Others
Language:zh-TW
Published: 2003
Online Access:http://ndltd.ncl.edu.tw/handle/zyvy23
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spelling ndltd-TW-091CYUT55000082018-06-25T06:06:27Z http://ndltd.ncl.edu.tw/handle/zyvy23 Synthetic Studies on the Key Intermediate of Potent Anti-tumor Natural Products-Saframycin A 抗癌天然物沙弗拉黴素(SaframycinA)重要中間體之合成研究 Meng-Tsung Li 李孟宗 碩士 朝陽科技大學 應用化學系碩士班 91 Saframycin A (1a) is one kind of natural products which show potent antitumor antibiotics. Due to the scant availability from natural sources and difficulty in cultivation, we make an attempt to synthsize derivatives of the Saframycin A (1a) by means of organic synthesis. The main purpose of this study is to utilize an inexpensive, exhibiting stereo-controlled substance, being a natural amino acid L-tyrosine as a starting material which could be transformed into the key intermediate 34b an optically active dizobicyclo [3.3.1] nonane. 34b may be further transformed to compound 33 which has been synthesized by Dr. E. J.Corey, and subsequently 33 was converted to Saframycin A (1a). none 卓重光 2003 學位論文 ; thesis 141 zh-TW
collection NDLTD
language zh-TW
format Others
sources NDLTD
description 碩士 === 朝陽科技大學 === 應用化學系碩士班 === 91 === Saframycin A (1a) is one kind of natural products which show potent antitumor antibiotics. Due to the scant availability from natural sources and difficulty in cultivation, we make an attempt to synthsize derivatives of the Saframycin A (1a) by means of organic synthesis. The main purpose of this study is to utilize an inexpensive, exhibiting stereo-controlled substance, being a natural amino acid L-tyrosine as a starting material which could be transformed into the key intermediate 34b an optically active dizobicyclo [3.3.1] nonane. 34b may be further transformed to compound 33 which has been synthesized by Dr. E. J.Corey, and subsequently 33 was converted to Saframycin A (1a).
author2 none
author_facet none
Meng-Tsung Li
李孟宗
author Meng-Tsung Li
李孟宗
spellingShingle Meng-Tsung Li
李孟宗
Synthetic Studies on the Key Intermediate of Potent Anti-tumor Natural Products-Saframycin A
author_sort Meng-Tsung Li
title Synthetic Studies on the Key Intermediate of Potent Anti-tumor Natural Products-Saframycin A
title_short Synthetic Studies on the Key Intermediate of Potent Anti-tumor Natural Products-Saframycin A
title_full Synthetic Studies on the Key Intermediate of Potent Anti-tumor Natural Products-Saframycin A
title_fullStr Synthetic Studies on the Key Intermediate of Potent Anti-tumor Natural Products-Saframycin A
title_full_unstemmed Synthetic Studies on the Key Intermediate of Potent Anti-tumor Natural Products-Saframycin A
title_sort synthetic studies on the key intermediate of potent anti-tumor natural products-saframycin a
publishDate 2003
url http://ndltd.ncl.edu.tw/handle/zyvy23
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AT lǐmèngzōng kàngáitiānránwùshāfúlāméisùsaframycinazhòngyàozhōngjiāntǐzhīhéchéngyánjiū
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