Scot M. Sutton, Sunil Pulletikurti, Huacan Lin, Ramanarayanan Krishnamurthy, Charles L. Liotta
{"title":"甲醛与酮糖和醛糖的非生物醛醇反应——通过甲醛反应合成糖的益生元意义","authors":"Scot M. Sutton, Sunil Pulletikurti, Huacan Lin, Ramanarayanan Krishnamurthy, Charles L. Liotta","doi":"10.1016/j.chempr.2025.102553","DOIUrl":null,"url":null,"abstract":"The aldol reactions of formaldehyde is the essence of the formose reaction, considered the leading prebiotic pathway for accessing sugars on the early Earth. However, the formose reaction produces an intractable mixture, and efforts to tame the reaction to selectively and efficiently form aldose sugars have been unsuccessful. We have undertaken an NMR-mechanistic study of the aldol reactions of excess formaldehyde with glycolaldehyde, dihydroxyacetone, erythrulose, and erythrose under mild conditions and show that the reaction pathway is dominated by the formation linear ketoses and eventual accumulation of branched ketoses. Formation of C4 and higher aldo-sugars were not observed, implying that neither carbonyl migrations nor retroaldol reactions are occurring. Our results suggest that (1) controlling the aldol reaction of formaldehyde to selectively produce linear aldoses appears unfeasible; and (2) the concept of the formose reaction as a prebiotic source of ribose on early Earth needs serious reconsideration, and other models/options should be explored.","PeriodicalId":268,"journal":{"name":"Chem","volume":"51 1","pages":""},"PeriodicalIF":19.1000,"publicationDate":"2025-04-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Abiotic aldol reactions of formaldehyde with ketoses and aldoses—Implications for the prebiotic synthesis of sugars by the formose reaction\",\"authors\":\"Scot M. Sutton, Sunil Pulletikurti, Huacan Lin, Ramanarayanan Krishnamurthy, Charles L. Liotta\",\"doi\":\"10.1016/j.chempr.2025.102553\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The aldol reactions of formaldehyde is the essence of the formose reaction, considered the leading prebiotic pathway for accessing sugars on the early Earth. However, the formose reaction produces an intractable mixture, and efforts to tame the reaction to selectively and efficiently form aldose sugars have been unsuccessful. We have undertaken an NMR-mechanistic study of the aldol reactions of excess formaldehyde with glycolaldehyde, dihydroxyacetone, erythrulose, and erythrose under mild conditions and show that the reaction pathway is dominated by the formation linear ketoses and eventual accumulation of branched ketoses. Formation of C4 and higher aldo-sugars were not observed, implying that neither carbonyl migrations nor retroaldol reactions are occurring. Our results suggest that (1) controlling the aldol reaction of formaldehyde to selectively produce linear aldoses appears unfeasible; and (2) the concept of the formose reaction as a prebiotic source of ribose on early Earth needs serious reconsideration, and other models/options should be explored.\",\"PeriodicalId\":268,\"journal\":{\"name\":\"Chem\",\"volume\":\"51 1\",\"pages\":\"\"},\"PeriodicalIF\":19.1000,\"publicationDate\":\"2025-04-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chem\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1016/j.chempr.2025.102553\",\"RegionNum\":1,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chem","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1016/j.chempr.2025.102553","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Abiotic aldol reactions of formaldehyde with ketoses and aldoses—Implications for the prebiotic synthesis of sugars by the formose reaction
The aldol reactions of formaldehyde is the essence of the formose reaction, considered the leading prebiotic pathway for accessing sugars on the early Earth. However, the formose reaction produces an intractable mixture, and efforts to tame the reaction to selectively and efficiently form aldose sugars have been unsuccessful. We have undertaken an NMR-mechanistic study of the aldol reactions of excess formaldehyde with glycolaldehyde, dihydroxyacetone, erythrulose, and erythrose under mild conditions and show that the reaction pathway is dominated by the formation linear ketoses and eventual accumulation of branched ketoses. Formation of C4 and higher aldo-sugars were not observed, implying that neither carbonyl migrations nor retroaldol reactions are occurring. Our results suggest that (1) controlling the aldol reaction of formaldehyde to selectively produce linear aldoses appears unfeasible; and (2) the concept of the formose reaction as a prebiotic source of ribose on early Earth needs serious reconsideration, and other models/options should be explored.
期刊介绍:
Chem, affiliated with Cell as its sister journal, serves as a platform for groundbreaking research and illustrates how fundamental inquiries in chemistry and its related fields can contribute to addressing future global challenges. It was established in 2016, and is currently edited by Robert Eagling.