Valérie Toussaint, Theresa Röper, Katarina Hricova, Irina Delidovich
{"title":"锡有机骨架催化外映异构合成稀有糖的研究","authors":"Valérie Toussaint, Theresa Röper, Katarina Hricova, Irina Delidovich","doi":"10.1016/j.crgsc.2025.100476","DOIUrl":null,"url":null,"abstract":"<div><div>Epimerization of readily available monosaccharides presents an atom-efficient approach to expand the portfolio of rare monosaccharides. Here, we report tin-organic frameworks (Sn-OF) as a highly selective catalyst for synthesis of rare monosaccharides, such as L-ribose, D-lyxose, D-talose, and L-quinovose, <em>via</em> epimerization reaction. Remarkable selectivity of 67–95 % for the epimerization products was achieved. The maximal yields obtained were 22 % for D-lyxose, 14 % for L-ribose, 15 % for D-talose, and 18 % for L-quinovose. Additionally, a correlation between the structure of the substrate and reaction rate was established, suggesting that the saccharides react in open-chain form, with the <em>cis</em>-orientation of OH-groups facilitating the epimerization. Moreover, it was shown that the catalyst can be reused in a second run. The catalytic epimerization results in a mixture of epimers, from which partial recovery of the substrate can be achieved through crystallization, as demonstrated for L-arabinose, D-galactose, and D-xylose.</div></div>","PeriodicalId":296,"journal":{"name":"Current Research in Green and Sustainable Chemistry","volume":"11 ","pages":"Article 100476"},"PeriodicalIF":0.0000,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Synthesis of rare sugars via epimerization catalyzed by tin-organic frameworks\",\"authors\":\"Valérie Toussaint, Theresa Röper, Katarina Hricova, Irina Delidovich\",\"doi\":\"10.1016/j.crgsc.2025.100476\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>Epimerization of readily available monosaccharides presents an atom-efficient approach to expand the portfolio of rare monosaccharides. Here, we report tin-organic frameworks (Sn-OF) as a highly selective catalyst for synthesis of rare monosaccharides, such as L-ribose, D-lyxose, D-talose, and L-quinovose, <em>via</em> epimerization reaction. Remarkable selectivity of 67–95 % for the epimerization products was achieved. The maximal yields obtained were 22 % for D-lyxose, 14 % for L-ribose, 15 % for D-talose, and 18 % for L-quinovose. Additionally, a correlation between the structure of the substrate and reaction rate was established, suggesting that the saccharides react in open-chain form, with the <em>cis</em>-orientation of OH-groups facilitating the epimerization. Moreover, it was shown that the catalyst can be reused in a second run. The catalytic epimerization results in a mixture of epimers, from which partial recovery of the substrate can be achieved through crystallization, as demonstrated for L-arabinose, D-galactose, and D-xylose.</div></div>\",\"PeriodicalId\":296,\"journal\":{\"name\":\"Current Research in Green and Sustainable Chemistry\",\"volume\":\"11 \",\"pages\":\"Article 100476\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2025-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Current Research in Green and Sustainable Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2666086525000323\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"Materials Science\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Current Research in Green and Sustainable Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2666086525000323","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"Materials Science","Score":null,"Total":0}
Synthesis of rare sugars via epimerization catalyzed by tin-organic frameworks
Epimerization of readily available monosaccharides presents an atom-efficient approach to expand the portfolio of rare monosaccharides. Here, we report tin-organic frameworks (Sn-OF) as a highly selective catalyst for synthesis of rare monosaccharides, such as L-ribose, D-lyxose, D-talose, and L-quinovose, via epimerization reaction. Remarkable selectivity of 67–95 % for the epimerization products was achieved. The maximal yields obtained were 22 % for D-lyxose, 14 % for L-ribose, 15 % for D-talose, and 18 % for L-quinovose. Additionally, a correlation between the structure of the substrate and reaction rate was established, suggesting that the saccharides react in open-chain form, with the cis-orientation of OH-groups facilitating the epimerization. Moreover, it was shown that the catalyst can be reused in a second run. The catalytic epimerization results in a mixture of epimers, from which partial recovery of the substrate can be achieved through crystallization, as demonstrated for L-arabinose, D-galactose, and D-xylose.