{"title":"[多催化反应的Pickering乳液策略]。","authors":"Kyohei Kanomata","doi":"10.1248/yakushi.25-00120","DOIUrl":null,"url":null,"abstract":"<p><p>Enantiomers of a chiral compound often exhibit distinct physiological activities, making enantioselective synthesis of chiral molecules a critical challenge in drug discovery. This study explored a novel strategy for converting racemic compounds into a single enantiomer using enzymes, with a focus on developing a methodology to access both enantiomers of chiral esters using a single lipase and enantioconvergent reactions of tertiary alcohols. The desired transformations were achieved by designing multi-catalytic systems that enabled lipases to combine with otherwise incompatible catalysts and reactants using Pickering emulsions as compartmentalized reaction media.</p>","PeriodicalId":23810,"journal":{"name":"Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan","volume":"145 10","pages":"833-842"},"PeriodicalIF":0.2000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Pickering Emulsion Strategy for Multi-Catalytic Reactions].\",\"authors\":\"Kyohei Kanomata\",\"doi\":\"10.1248/yakushi.25-00120\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Enantiomers of a chiral compound often exhibit distinct physiological activities, making enantioselective synthesis of chiral molecules a critical challenge in drug discovery. This study explored a novel strategy for converting racemic compounds into a single enantiomer using enzymes, with a focus on developing a methodology to access both enantiomers of chiral esters using a single lipase and enantioconvergent reactions of tertiary alcohols. The desired transformations were achieved by designing multi-catalytic systems that enabled lipases to combine with otherwise incompatible catalysts and reactants using Pickering emulsions as compartmentalized reaction media.</p>\",\"PeriodicalId\":23810,\"journal\":{\"name\":\"Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan\",\"volume\":\"145 10\",\"pages\":\"833-842\"},\"PeriodicalIF\":0.2000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1248/yakushi.25-00120\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"PHARMACOLOGY & PHARMACY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Yakugaku zasshi : Journal of the Pharmaceutical Society of Japan","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1248/yakushi.25-00120","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"PHARMACOLOGY & PHARMACY","Score":null,"Total":0}
[Pickering Emulsion Strategy for Multi-Catalytic Reactions].
Enantiomers of a chiral compound often exhibit distinct physiological activities, making enantioselective synthesis of chiral molecules a critical challenge in drug discovery. This study explored a novel strategy for converting racemic compounds into a single enantiomer using enzymes, with a focus on developing a methodology to access both enantiomers of chiral esters using a single lipase and enantioconvergent reactions of tertiary alcohols. The desired transformations were achieved by designing multi-catalytic systems that enabled lipases to combine with otherwise incompatible catalysts and reactants using Pickering emulsions as compartmentalized reaction media.