{"title":"从 D-(-)-奎宁酸合成 L-(+)-奎宁酸","authors":"Johnny Nguyen, Sandeep Bhosale, Andrew J. Bennet","doi":"10.1139/cjc-2023-0139","DOIUrl":null,"url":null,"abstract":"Here, we report an efficient synthesis of L-(+)-quinic acid from the natural product D-(–)-quinic acid in a twelve-step sequence. The key steps involve the kinetic controlled selective protection of a lactone intermediate and the inversion of two stereocentres: the C-3 and C-5 hydroxyl of the quinic acid core using optimized oxidation-reduction conditions.","PeriodicalId":9420,"journal":{"name":"Canadian Journal of Chemistry","volume":"14 5","pages":""},"PeriodicalIF":1.1000,"publicationDate":"2023-11-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"A synthesis of L-(+)-quinic acid from D-(–)-quinic acid\",\"authors\":\"Johnny Nguyen, Sandeep Bhosale, Andrew J. Bennet\",\"doi\":\"10.1139/cjc-2023-0139\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Here, we report an efficient synthesis of L-(+)-quinic acid from the natural product D-(–)-quinic acid in a twelve-step sequence. The key steps involve the kinetic controlled selective protection of a lactone intermediate and the inversion of two stereocentres: the C-3 and C-5 hydroxyl of the quinic acid core using optimized oxidation-reduction conditions.\",\"PeriodicalId\":9420,\"journal\":{\"name\":\"Canadian Journal of Chemistry\",\"volume\":\"14 5\",\"pages\":\"\"},\"PeriodicalIF\":1.1000,\"publicationDate\":\"2023-11-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Canadian Journal of Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1139/cjc-2023-0139\",\"RegionNum\":4,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Canadian Journal of Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1139/cjc-2023-0139","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
A synthesis of L-(+)-quinic acid from D-(–)-quinic acid
Here, we report an efficient synthesis of L-(+)-quinic acid from the natural product D-(–)-quinic acid in a twelve-step sequence. The key steps involve the kinetic controlled selective protection of a lactone intermediate and the inversion of two stereocentres: the C-3 and C-5 hydroxyl of the quinic acid core using optimized oxidation-reduction conditions.
期刊介绍:
Published since 1929, the Canadian Journal of Chemistry reports current research findings in all branches of chemistry. It includes the traditional areas of analytical, inorganic, organic, and physical-theoretical chemistry and newer interdisciplinary areas such as materials science, spectroscopy, chemical physics, and biological, medicinal and environmental chemistry. Articles describing original research are welcomed.