回顾性分析
化学
天然产物
生化工程
二萜
药物发现
自然(考古学)
组合化学
全合成
纳米技术
有机化学
工程类
生物化学
材料科学
考古
历史
作者
Mohamed F. Elmansy,Rita M. Borik,Rizk E. Khidre
标识
DOI:10.2174/1385272827666230512114730
摘要
Abstract: Nature is an inspiring source in drug discovery which constantly reveals new complex chemical structures of natural products that inherit attractive chemical challenges for organic chemists to synthesize them. Taxol is a unique natural product that impressive biological properties and a very tempting chemical structure that motivated organic chemists all over the world to enter the race for synthesizing it. The total synthesis of this highly oxygenated diterpene was completed by 11 different research groups starting from Holton (1994) to Chida (2022). This review article demonstrates the various retrosynthetic analysis of Taxol, the actual synthetic routes to it and highlights the key steps in each synthesis. It also provides a critical review of the advantages and disadvantages in all the synthetic routes in terms of number of steps, yields and the synthetic challenges.
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