Wei-Nan Xu, Ya-Dong Gao, Ping Su, Luqi Huang, Zhao-Lin He* and Li-Cheng Yang*,
{"title":"酶催化 C(sp3)-H Amination 的研究进展","authors":"Wei-Nan Xu, Ya-Dong Gao, Ping Su, Luqi Huang, Zhao-Lin He* and Li-Cheng Yang*, ","doi":"10.1021/acscatal.4c0494710.1021/acscatal.4c04947","DOIUrl":null,"url":null,"abstract":"<p >Amine structures are widely present in various biologically active natural products, drug molecules, and material structures. Among the various strategies of amine synthesis, C(sp<sup>3</sup>)–H amination has become a powerful strategy due to its atom economy and multiple potential reaction sites compared with conventional amine synthesis methods. Due to the advantages of high catalytic efficiency, high selectivity, environmental friendliness, and high modifiability of the enzyme, the enzymatic C(sp<sup>3</sup>)–H amination is of great research significance. However, it was not until recent years that natural enzymes capable of catalyzing the amination of C(sp<sup>3</sup>)–H bonds were discovered. Modifying enzymes to confer unnatural C(sp<sup>3</sup>)–H amination activity holds great potential. In the past decade, a series of protocols for the amination of C(sp<sup>3</sup>)–H bonds using engineered enzymes have been developed, several of which showed comparable properties to those of natural enzymes.</p>","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":null,"pages":null},"PeriodicalIF":11.3000,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Progress in Enzyme-Catalyzed C(sp3)–H Amination\",\"authors\":\"Wei-Nan Xu, Ya-Dong Gao, Ping Su, Luqi Huang, Zhao-Lin He* and Li-Cheng Yang*, \",\"doi\":\"10.1021/acscatal.4c0494710.1021/acscatal.4c04947\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Amine structures are widely present in various biologically active natural products, drug molecules, and material structures. Among the various strategies of amine synthesis, C(sp<sup>3</sup>)–H amination has become a powerful strategy due to its atom economy and multiple potential reaction sites compared with conventional amine synthesis methods. Due to the advantages of high catalytic efficiency, high selectivity, environmental friendliness, and high modifiability of the enzyme, the enzymatic C(sp<sup>3</sup>)–H amination is of great research significance. However, it was not until recent years that natural enzymes capable of catalyzing the amination of C(sp<sup>3</sup>)–H bonds were discovered. Modifying enzymes to confer unnatural C(sp<sup>3</sup>)–H amination activity holds great potential. In the past decade, a series of protocols for the amination of C(sp<sup>3</sup>)–H bonds using engineered enzymes have been developed, several of which showed comparable properties to those of natural enzymes.</p>\",\"PeriodicalId\":9,\"journal\":{\"name\":\"ACS Catalysis \",\"volume\":null,\"pages\":null},\"PeriodicalIF\":11.3000,\"publicationDate\":\"2024-09-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Catalysis \",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acscatal.4c04947\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, PHYSICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acscatal.4c04947","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
Amine structures are widely present in various biologically active natural products, drug molecules, and material structures. Among the various strategies of amine synthesis, C(sp3)–H amination has become a powerful strategy due to its atom economy and multiple potential reaction sites compared with conventional amine synthesis methods. Due to the advantages of high catalytic efficiency, high selectivity, environmental friendliness, and high modifiability of the enzyme, the enzymatic C(sp3)–H amination is of great research significance. However, it was not until recent years that natural enzymes capable of catalyzing the amination of C(sp3)–H bonds were discovered. Modifying enzymes to confer unnatural C(sp3)–H amination activity holds great potential. In the past decade, a series of protocols for the amination of C(sp3)–H bonds using engineered enzymes have been developed, several of which showed comparable properties to those of natural enzymes.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.