New Methods for the Stereoselective Synthesis of Organic Compounds

有机化合物立体选择性合成的新方法

基本信息

  • 批准号:
    RGPIN-2014-06438
  • 负责人:
  • 金额:
    $ 12.02万
  • 依托单位:
  • 依托单位国家:
    加拿大
  • 项目类别:
    Discovery Grants Program - Individual
  • 财政年份:
    2018
  • 资助国家:
    加拿大
  • 起止时间:
    2018-01-01 至 2019-12-31
  • 项目状态:
    已结题

项目摘要

Most important molecules found in nature (enzymes, proteins, RNA, DNA, etc.) are chiral and cannot be superimposed upon their mirror image. Yet, these compounds are the most challenging to selectively synthesize due to their inherent similarity between various chemical structures. Normally, when a chiral molecule is produced in the laboratory, its synthesis produces a mixture containing equal amounts of two enantiomer forms, but while one form may be beneficial to health, the other may be harmful. On the other hand, small heteroaromatic rings are of central importance in the development of novel synthetic protein ligands that will eventually evolve into novel drugs. It is estimated that over 3,000 of these molecules are still unknown! The plethora of successful methodologies available in organic synthesis has reached an impressive number, but there is still a long way to go to synthesize any molecule using highly efficient methods having minimal environmental impact. **The specific aim of our research will be directed towards the development of new and efficient methods for the selective (regio-, chemo-, enantio- and/or diasteroselective) synthesis of organic compounds containing mostly carbon, hydrogen, oxygen and nitrogen. As organic chemists, we always strive not only to improve existing synthetic methods, but also to develop new and more effective ones. To that effect, more powerful, greener, and protecting-group-free are still needed. This area of organic chemistry is of primary importance due to today's necessity for enantiomerically pure compounds in a variety of related disciplines (pharmaceuticals, agrochemicals, biology, material sciences, biochemistry, food sciences, etc.). **In order to achieve this, we will develop novel tools (reagents and catalysts) to help control the specificity of a given chemical transformation. Among the priorities, cyclopropane synthesis and functionalization, novel heterocycle synthesis and functionalization, highly chemoselective transformations using amides, as well as catalytic amide synthesis are the most important themes. We will also concentrate our efforts on understanding the fundamental mechanistic implications of the newly developed transformations. This will allow us to build upon observations and push the chemistry to higher limits. Finally, the synthesis of complex natural products will be pursued, since this is the ultimate ground to test the efficiency of new synthetic methodologies. Catalysis, which is featured as one of the 12 principles of Green chemistry and as one of the key strategies to use in Green chemical processes, will play a central role in the development of new methods.**Overall, the fruits of our research will be extremely important for both the academic and industrial sectors, because chiral, non-racemic compounds are critical intermediates that will lead to the development of new products in fields as diverse as pharmaceutical science, agrochemical science, biology, biochemistry, food science, materials sciences, pharmacology and medicine. Considering that several chemistry-related companies are based in the greater Montreal area, we anticipate that our research will naturally strengthen and complement their existing R&D programs, thus help them hone their competitive edge in the global economy. As well, a new generation of highly qualified scientists possessing unique skills and a modern mindset on organic chemistry and green practices will be perfectly trained to join the workforce and to ensure a flow of unique expertise into the marketplace. In addition, the potential for discoveries that will emerge from our research will open the door to innovation, which, ultimately, will create a healthier and cleaner environment for the Canadian population at large.
自然界中发现的最重要的分子(酶、蛋白质、RNA、DNA等)都是手性的,不能叠加在它们的镜像上。然而,这些化合物是最具挑战性的选择性合成,因为它们在不同的化学结构之间具有内在的相似性。通常,当在实验室中生产手性分子时,其合成会产生含有等量两种对映体形式的混合物,但其中一种形式可能对健康有益,另一种可能有害。另一方面,小的杂芳环在开发新的合成蛋白质配体方面起着核心作用,这些配体最终将进化成新的药物。据估计,这些分子中有3000多个仍然未知!有机合成中的许多成功方法已经达到了令人印象深刻的数量,但要用对环境影响最小的高效方法来合成任何分子,还有很长的路要走。**我们研究的具体目标将是开发新的有效方法来选择性(区域、化学、对映体和/或非对映选择性)合成主要含有碳、氢、氧和氮的有机化合物。作为有机化学家,我们不仅努力改进现有的合成方法,而且还努力开发新的和更有效的方法。为此,仍然需要更强大、更环保、更无保护群体的环境。有机化学的这一领域至关重要,因为当今在各种相关学科(药学、农用化学品、生物学、材料科学、生物化学、食品科学等)中都需要具有对映体纯度的化合物。**为了实现这一点,我们将开发新的工具(试剂和催化剂)来帮助控制给定化学转化的特异性。其中,环丙烷的合成和功能化、新型杂环的合成和功能化、使用酰胺的高化学选择性转化以及催化酰胺合成是最重要的主题。我们还将集中精力理解新发展的转变的基本机制含义。这将允许我们建立在观察的基础上,并将化学作用推向更高的极限。最后,将继续进行复杂天然产物的合成,因为这是测试新合成方法效率的最终基础。催化是绿色化学的12项原则之一,也是绿色化学过程中使用的关键策略之一,它将在新方法的开发中发挥核心作用。**总的来说,我们的研究成果对学术和工业部门都非常重要,因为手性、非外消旋化合物是关键的中间体,将导致制药科学、农业化学、生物、生物化学、食品科学、材料科学、药理学和医药等领域的新产品开发。考虑到几家化学相关公司的总部设在大蒙特利尔地区,我们预计我们的研究将自然加强和补充他们现有的研发计划,从而帮助他们磨练在全球经济中的竞争优势。此外,在有机化学和绿色实践方面拥有独特技能和现代思维的新一代高素质科学家将接受完美的培训,以加入劳动力大军,并确保独特的专业知识流入市场。此外,我们的研究将带来发现的潜力,这将为创新打开大门,最终将为加拿大广大人口创造一个更健康、更清洁的环境。

项目成果

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Charette, Andre其他文献

Microstructure and rheological behavior of grain refined and modified semi-solid A356 Al-Si slurries
  • DOI:
    10.1016/j.actamat.2006.03.016
  • 发表时间:
    2006-08-01
  • 期刊:
  • 影响因子:
    9.4
  • 作者:
    Nafisi, Shahrooz;Lashkari, Omid;Charette, Andre
  • 通讯作者:
    Charette, Andre
A sensitivity function-based conjugate gradient method for optical tomography with the frequency-domain equation of radiative transfer

Charette, Andre的其他文献

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{{ truncateString('Charette, Andre', 18)}}的其他基金

New Methods for the Stereoselective Synthesis of Organic Compounds
有机化合物立体选择性合成的新方法
  • 批准号:
    RGPIN-2019-06113
  • 财政年份:
    2019
  • 资助金额:
    $ 12.02万
  • 项目类别:
    Discovery Grants Program - Individual
NSERC CREATE Training Program in Continuous Flow Science
NSERC CREATE 连续流科学培训计划
  • 批准号:
    449307-2014
  • 财政年份:
    2019
  • 资助金额:
    $ 12.02万
  • 项目类别:
    Collaborative Research and Training Experience

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  • 批准号:
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  • 批准年份:
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