The Total Synthesis of 6-Hydroxypunctaporonin E
6-羟基点孔蛋白E的全合成
基本信息
- 批准号:8283194
- 负责人:
- 金额:$ 0.79万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2010
- 资助国家:美国
- 起止时间:2010-07-19 至 2012-07-18
- 项目状态:已结题
- 来源:
- 关键词:AcidsAlder plantAntibioticsBacillus subtilisBacteriaBacterial InfectionsBiologicalBiological FactorsChemistryDevelopmentDiels Alder reactionEvaluationFutureGenus staphylococcusGoalsGrowthMedicinePharmaceutical PreparationsPropertyResearchResistance developmentRoutedesignfungusnovelpublic health relevance
项目摘要
DESCRIPTION (provided by applicant): The goal of the proposed research is to define the first synthetic route toward 6-hydroxypunctaporonin E, a polycyclic natural product. 6-Hydroxypunctaporonin E was isolated from the fungicolous fungi Pestalotiopsis disseminata, collected in the state of Georgia, and was shown to have antibiotic properties inhibiting the growth of Bacillus subtilis and Staphylococcus aureas.[1] The proposed synthetic route includes an unusual example of the Diels-Alder reaction between a vinylcyclobutene and a dihydrofuranone. Included with the synthetic goal are the design of a novel chiral Lewis acid for Diels-Alder chemistry, and the study of a 6-hydroxypunctaporon E conjugate.
PUBLIC HEALTH RELEVANCE: The development of broadly applicable antibiotic medicines is one of mankind's noteworthy accomplishments of the last century. Unfortunately, bacteria have begun to develop resistance to common medications used in the treatment of bacterial infections. As a result there is a continued need for research into the synthesis and biological evaluation of new compounds with antibiotic properties, to better understand their potential as new antibiotics of the future.
描述(由申请人提供):拟议研究的目标是确定6-羟基聚甲钙蛋白E的第一条合成路线,这是一种多环天然产物。6-羟基聚磷蛋白E是从美国乔治亚州收集的广布拟盘多毛孢真菌中分离出来的,具有抑制枯草芽孢杆菌和金黄色葡萄球菌生长的抗生素特性提出的合成路线包括乙烯基环丁烯和二氢呋喃酮之间的Diels-Alder反应的一个不寻常的例子。合成目标包括设计一种用于Diels-Alder化学的新型手性Lewis酸,以及研究6-羟基磷酸E缀合物。
项目成果
期刊论文数量(1)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Martin John McLaughlin其他文献
Martin John McLaughlin的其他文献
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