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Enantioselective Conversion of Achiral Diketones and Triketones for Shortened Bioactive Molecule Synthesis

Enantioselective Conversion of Achiral Diketones and Triketones for Shortened Bioactive Molecule Synthesis
非手性二酮和三酮的对映选择性转化以缩短生物活性分子的合成
批准号:
245372425
负责人:
Professor Dr. Thomas Nugent
金额:
$0.0万
依托单位国家:
德国
项目类别:
Research Grants
财政年份:
2013
资助国家:
德国
项目状态:
已结题
起止时间:
2012-12-31 至 2018-12-31

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中文摘要
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英文摘要
The constant demand for new and more complex enantiopure pharmaceutical drugs has made enantioselective organic methodology a high growth area, which is supported by academic granting agencies. In this context, the discovery and development of sustainable enantioselective methods (reduced environmental impact chemistry) is a current and ever increasing theme within chemistry. In this context water is an interesting solvent because of its availability and potential for allowing the development of green methods. This project fits into the above noted themes and is a request to develop promising organocatalysts for aldol and related reactions. The forwarding looking goal of this project is to allow greater design flexibility with improved efficiency for the synthesis of pharmaceutical drugs and natural products with reduced environmental impact.
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The First Broad Examination of Michael Reactions in the Presence of a Diverse Array of Acidic Spectator Functional Groups: Enantioselective Synthesis
Enantioselective Ammonium Enolate Based Michael-Henry and Michael-Henry-Aldol Cascade Reactions: Development, Mechanistic Insight, and Applications for Morphine Family Analgesics
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