由乙醇酸合成抗SARS3CL蛋白抑制[]之研究

碩士 === 國立清華大學 === 化學系 === 93 === The main idea of this thesis is to synthesize the pharmaceutical Anti-SARS moleculars by asymmetric reactions of 1,3-dioxolan-4-ones derived from camphorsulfonamide. Most of the pharmaceutical Anti-SARS molecular were considered as an AG7088 core structure with diver...

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Bibliographic Details
Main Author: 呂和榮
Other Authors: 汪炳鈞
Format: Others
Language:zh-TW
Published: 2005
Online Access:http://ndltd.ncl.edu.tw/handle/45093448939732658895