Yan Wang, Zhongjie Wang, Hui Luo, Guohui Wang, Zhendong Shi, Yinfeng Ma, Jianglong Wu, Dianjun Li and Jinhui Yang
{"title":"NaI/NPh3或NaI/PPh3在水中介导的β-二羰基化合物的可见光驱动α-羟基化反应","authors":"Yan Wang, Zhongjie Wang, Hui Luo, Guohui Wang, Zhendong Shi, Yinfeng Ma, Jianglong Wu, Dianjun Li and Jinhui Yang","doi":"10.1039/D4QO01169D","DOIUrl":null,"url":null,"abstract":"<p >The synthesis of α-hydroxy carbonyl compounds through the electron donor–acceptor (EDA) complex system in an aqueous phase has not been reported previously. This report presents a novel and efficient EDA complex system employing β-dicarbonyl substrates that do not require previous installation, NaI and inexpensive NPh<small><sub>3</sub></small>. The purpose of constructing this EDA complex is to improve and advance the EDA photocatalytic system in the aqueous phase, while maintaining tolerance to oxygen. The complexes were used to realize the hydrogen evolution reaction and hydration–hydroxylation of β-dicarbonyl derivatives in a non-homogeneous system using water as the solvent and oxygen source. The reaction exhibits broad substrate compatibility, does not need phase-transfer catalysts or additional oxidants, is alkali-free and metal-free, and allows microreactor gram-scale preparation. The reaction not only is suitable for liquid matrices but also can achieve the desired yield through an increase in the concentration of the green solvent ethanol, when the light transfer is obstructed by insoluble solid matrices.</p>","PeriodicalId":97,"journal":{"name":"Organic Chemistry Frontiers","volume":" 19","pages":" 5524-5531"},"PeriodicalIF":4.7000,"publicationDate":"2024-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Visible-light-driven α-hydroxylation of β-dicarbonyl compounds mediated by NaI/NPh3 or NaI/PPh3 in water†\",\"authors\":\"Yan Wang, Zhongjie Wang, Hui Luo, Guohui Wang, Zhendong Shi, Yinfeng Ma, Jianglong Wu, Dianjun Li and Jinhui Yang\",\"doi\":\"10.1039/D4QO01169D\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >The synthesis of α-hydroxy carbonyl compounds through the electron donor–acceptor (EDA) complex system in an aqueous phase has not been reported previously. This report presents a novel and efficient EDA complex system employing β-dicarbonyl substrates that do not require previous installation, NaI and inexpensive NPh<small><sub>3</sub></small>. The purpose of constructing this EDA complex is to improve and advance the EDA photocatalytic system in the aqueous phase, while maintaining tolerance to oxygen. The complexes were used to realize the hydrogen evolution reaction and hydration–hydroxylation of β-dicarbonyl derivatives in a non-homogeneous system using water as the solvent and oxygen source. The reaction exhibits broad substrate compatibility, does not need phase-transfer catalysts or additional oxidants, is alkali-free and metal-free, and allows microreactor gram-scale preparation. The reaction not only is suitable for liquid matrices but also can achieve the desired yield through an increase in the concentration of the green solvent ethanol, when the light transfer is obstructed by insoluble solid matrices.</p>\",\"PeriodicalId\":97,\"journal\":{\"name\":\"Organic Chemistry Frontiers\",\"volume\":\" 19\",\"pages\":\" 5524-5531\"},\"PeriodicalIF\":4.7000,\"publicationDate\":\"2024-08-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Chemistry Frontiers\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.rsc.org/en/content/articlelanding/2024/qo/d4qo01169d\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, ORGANIC\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2024/qo/d4qo01169d","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
Visible-light-driven α-hydroxylation of β-dicarbonyl compounds mediated by NaI/NPh3 or NaI/PPh3 in water†
The synthesis of α-hydroxy carbonyl compounds through the electron donor–acceptor (EDA) complex system in an aqueous phase has not been reported previously. This report presents a novel and efficient EDA complex system employing β-dicarbonyl substrates that do not require previous installation, NaI and inexpensive NPh3. The purpose of constructing this EDA complex is to improve and advance the EDA photocatalytic system in the aqueous phase, while maintaining tolerance to oxygen. The complexes were used to realize the hydrogen evolution reaction and hydration–hydroxylation of β-dicarbonyl derivatives in a non-homogeneous system using water as the solvent and oxygen source. The reaction exhibits broad substrate compatibility, does not need phase-transfer catalysts or additional oxidants, is alkali-free and metal-free, and allows microreactor gram-scale preparation. The reaction not only is suitable for liquid matrices but also can achieve the desired yield through an increase in the concentration of the green solvent ethanol, when the light transfer is obstructed by insoluble solid matrices.
期刊介绍:
Organic Chemistry Frontiers is an esteemed journal that publishes high-quality research across the field of organic chemistry. It places a significant emphasis on studies that contribute substantially to the field by introducing new or significantly improved protocols and methodologies. The journal covers a wide array of topics which include, but are not limited to, organic synthesis, the development of synthetic methodologies, catalysis, natural products, functional organic materials, supramolecular and macromolecular chemistry, as well as physical and computational organic chemistry.