{"title":"[金属-二膦]催化的 β-氨基 β-取代丙烯酸酯的不对称加氢反应:实用文献综述","authors":"Michel Stephan*, Marko Jeran and Barbara Mohar, ","doi":"10.1021/acs.oprd.3c00333","DOIUrl":null,"url":null,"abstract":"<p >Transition-metal-complex-catalyzed asymmetric hydrogenation of archetypal β-amido β-(methyl or phenyl)acrylates (and close derivatives) into the corresponding enantioenriched β-amido propionates is reviewed. The literature reports (including patents) on efficient enantiopure P,P-ligand-enabled catalytic systems─wherein the P,P-ligand is a <i>cis</i>-chelating diphosphine─are juxtaposed under their disclosed testing conditions per substrate along with the scored enantioselectivity. Such a listing clearly reveals their relative performance and constitutes a practical guide to inspire future development.</p>","PeriodicalId":55,"journal":{"name":"Organic Process Research & Development","volume":"28 1","pages":"11–25"},"PeriodicalIF":3.1000,"publicationDate":"2023-12-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Metal–Diphosphine]-Catalyzed Asymmetric Hydrogenation of β-Amido β-Substituted Acrylates: A Practical Literature Overview\",\"authors\":\"Michel Stephan*, Marko Jeran and Barbara Mohar, \",\"doi\":\"10.1021/acs.oprd.3c00333\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Transition-metal-complex-catalyzed asymmetric hydrogenation of archetypal β-amido β-(methyl or phenyl)acrylates (and close derivatives) into the corresponding enantioenriched β-amido propionates is reviewed. The literature reports (including patents) on efficient enantiopure P,P-ligand-enabled catalytic systems─wherein the P,P-ligand is a <i>cis</i>-chelating diphosphine─are juxtaposed under their disclosed testing conditions per substrate along with the scored enantioselectivity. Such a listing clearly reveals their relative performance and constitutes a practical guide to inspire future development.</p>\",\"PeriodicalId\":55,\"journal\":{\"name\":\"Organic Process Research & Development\",\"volume\":\"28 1\",\"pages\":\"11–25\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2023-12-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Process Research & Development\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.oprd.3c00333\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Process Research & Development","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.oprd.3c00333","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
[Metal–Diphosphine]-Catalyzed Asymmetric Hydrogenation of β-Amido β-Substituted Acrylates: A Practical Literature Overview
Transition-metal-complex-catalyzed asymmetric hydrogenation of archetypal β-amido β-(methyl or phenyl)acrylates (and close derivatives) into the corresponding enantioenriched β-amido propionates is reviewed. The literature reports (including patents) on efficient enantiopure P,P-ligand-enabled catalytic systems─wherein the P,P-ligand is a cis-chelating diphosphine─are juxtaposed under their disclosed testing conditions per substrate along with the scored enantioselectivity. Such a listing clearly reveals their relative performance and constitutes a practical guide to inspire future development.
期刊介绍:
The journal Organic Process Research & Development serves as a communication tool between industrial chemists and chemists working in universities and research institutes. As such, it reports original work from the broad field of industrial process chemistry but also presents academic results that are relevant, or potentially relevant, to industrial applications. Process chemistry is the science that enables the safe, environmentally benign and ultimately economical manufacturing of organic compounds that are required in larger amounts to help address the needs of society. Consequently, the Journal encompasses every aspect of organic chemistry, including all aspects of catalysis, synthetic methodology development and synthetic strategy exploration, but also includes aspects from analytical and solid-state chemistry and chemical engineering, such as work-up tools,process safety, or flow-chemistry. The goal of development and optimization of chemical reactions and processes is their transfer to a larger scale; original work describing such studies and the actual implementation on scale is highly relevant to the journal. However, studies on new developments from either industry, research institutes or academia that have not yet been demonstrated on scale, but where an industrial utility can be expected and where the study has addressed important prerequisites for a scale-up and has given confidence into the reliability and practicality of the chemistry, also serve the mission of OPR&D as a communication tool between the different contributors to the field.