Amino Acids and Peptides Organocatalysts: A Brief Overview on Its Evolution and Applications in Organic Asymmetric Synthesis

IF 0.9 Q4 CHEMISTRY, PHYSICAL Current Organocatalysis Pub Date : 2020-11-17 DOI:10.2174/2213337207999201117093848
Kantharaju Kamanna
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引用次数: 3

Abstract

This review highlights the application of biopolymers of natural α-amino acids and its derived wild-type peptides employed as organocatalysts for the asymmetric synthesis of various important compounds published by researchers across the globe. The α-amino acid with L-configuration is available commercially in the pure form and plays a crucial role in enantioselective chiral molecule synthesis. Out of twenty natural amino acids, only one secondary amine-containing proline amino acid exhibited revolution in the field of organocatalysis because of its rigid structure and the formation of an imine like transition state during the reaction, which leads to more stereoselectivity. Hence, it is referred to as a simple enzyme in organocatalyst. Chiral enantioselective organic molecule synthesis has been further discussed by employing oligopeptides derived from the natural amino acids as a robust biocatalyst that replaced enzyme catalysts. The di-, tri, tetra-, penta- and oligopeptide derived from the natural amino acids are demonstrated as a potential organocatalyst, whose catalytic activity and mechanistic pathways are reviewed in the present paper. Several choices of organocatalyst are developed to achieve a facile and efficient stereoselective synthesis of many complex natural products with optically pure isomer. Subsequently, the researcher developed green and sustainable heterogeneous catalytic system containing organocatalyst immobilized onto solid inorganic support or porous material for accelerating reaction rate with asymmetric one isomer product through the heterogeneous phase. Further, researchers developed heterogeneous organocatalysts-Metal-Organic Frameworks (MOFs) that emerged as alternative simple and facile heterogeneous catalysts for the bulk production and flow reactor for enantioselective synthesis. This review compiled many outstanding discoveries in organocatalysts derivative of amino acids, peptides and heterogenized-MOFs employed for many organic transformations in research and industrial applications.
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氨基酸和多肽有机催化剂的发展及其在有机不对称合成中的应用综述
本文综述了国际上已发表的天然α-氨基酸生物聚合物及其衍生的野生型多肽作为有机催化剂在不对称合成各种重要化合物中的应用。具有l构型的α-氨基酸在商业上以纯形式存在,在对映选择性手性分子合成中起着至关重要的作用。在20种天然氨基酸中,只有一种含脯氨酸的仲胺氨基酸在有机催化领域表现出革命性的作用,因为它的刚性结构和在反应过程中形成类似亚胺的过渡态,具有较高的立体选择性。因此,它在有机催化剂中被称为简单的酶。手性对映选择性有机分子的合成已经通过使用天然氨基酸衍生的寡肽作为替代酶催化剂的强大生物催化剂得到了进一步的讨论。从天然氨基酸中提取的二肽、三肽、四肽、五肽和寡肽是一种潜在的有机催化剂,本文对其催化活性和机理途径进行了综述。开发了几种有机催化剂,以实现许多具有光学纯异构体的复杂天然产物的简单而有效的立体选择合成。随后,研究人员开发了绿色可持续的多相催化体系,将有机催化剂刺激到固体无机载体或多孔材料上,通过多相相加速与不对称单异构体产物的反应速率。此外,研究人员还开发了非均相有机催化剂-金属有机框架(mof),作为批量生产和流动反应器中对映体选择性合成的简单而方便的非均相催化剂。本文综述了在研究和工业应用中用于许多有机转化的氨基酸衍生物、多肽和多相化mof的有机催化剂方面的许多突出发现。
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来源期刊
Current Organocatalysis
Current Organocatalysis CHEMISTRY, PHYSICAL-
CiteScore
2.00
自引率
0.00%
发文量
28
期刊介绍: Current Organocatalysis is an international peer-reviewed journal that publishes significant research in all areas of organocatalysis. The journal covers organo homogeneous/heterogeneous catalysis, innovative mechanistic studies and kinetics of organocatalytic processes focusing on practical, theoretical and computational aspects. It also includes potential applications of organocatalysts in the fields of drug discovery, synthesis of novel molecules, synthetic method development, green chemistry and chemoenzymatic reactions. This journal also accepts papers on methods, reagents, and mechanism of a synthetic process and technology pertaining to chemistry. Moreover, this journal features full-length/mini review articles within organocatalysis and synthetic chemistry. It is the premier source of organocatalysis and synthetic methods related information for chemists, biologists and engineers pursuing research in industry and academia.
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