含磷天然产物fosmidomycin和FR900098的优化合成

IF 1.4 4区 化学 Q4 CHEMISTRY, INORGANIC & NUCLEAR Phosphorus, Sulfur, and Silicon and the Related Elements Pub Date : 2023-01-01 DOI:10.1080/10426507.2023.2173756
Xin Wu , Hongrui Ping , Chunlin Song , Jiang Duan , Aidong Zhang
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引用次数: 1

摘要

Fosmidomycin及其乙酰类似物FR900098是植物和大多数细菌在类异戊二烯生物合成的2- c -甲基- d -赤藓糖醇4-磷酸(MEP)途径中对IspC酶具有抑制活性的两种含磷天然产物。本工作提出了一种利用现成原料化学合成磷霉素和FR900098的简便途径。通过对Michaelis-Becker反应和酰化关键步骤的反应条件进行优化,得到了福米霉素和FR900098的单钠盐,6个步骤的产率分别为60%和66%。这一统一的路线为报道的方法提供了另一种选择,使两种有价值的化合物的合成具有可扩展性和低成本,在开发新的抗疟疾药物和杀虫剂方面具有应用潜力。
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Optimization synthesis of phosphorous-containing natural products fosmidomycin and FR900098

Fosmidomycin and its acetyl analogue FR900098 are two phosphorus-containing natural products with inhibitory activity against IspC enzyme in the 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway of isoprenoid biosynthesis in plants and most bacteria. This work presents a facile route for the chemical synthesis of fosmidomycin and FR900098 using readily available raw materials. Through optimizing reaction conditions of the key steps of Michaelis-Becker reaction and acylation, the monosodium salts of fosmidomycin and FR900098 were obtained in yields of 60% and 66%, respectively, over six steps in the route. This unified route provides an alternative to the reported methods and makes it possible to synthesize the two valuable compounds with scalability and low cost, having the potential for application in developing new antimalarial drugs and pesticides.

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来源期刊
CiteScore
2.60
自引率
7.70%
发文量
103
审稿时长
2.1 months
期刊介绍: Phosphorus, Sulfur, and Silicon and the Related Elements is a monthly publication intended to disseminate current trends and novel methods to those working in the broad and interdisciplinary field of heteroatom chemistry.
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