{"title":"Eutyscoparol A 和 Violaceoid C 的全合成","authors":"","doi":"10.1002/ajoc.202400148","DOIUrl":null,"url":null,"abstract":"<div><p>The total syntheses of eutyscoparol A and violaceoid C <em>via</em> violaceoid A, have been accomplished including the improved total syntheses of violaceoid A and violaceoid B. This synthetic method, which employed the desymmetrization of a symmetric diol, enabled divergent access to other violaceoids, eutyscoparols, and their derivatives.</p></div>","PeriodicalId":130,"journal":{"name":"Asian Journal of Organic Chemistry","volume":"13 7","pages":"Article e202400148"},"PeriodicalIF":2.8000,"publicationDate":"2024-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ajoc.202400148","citationCount":"0","resultStr":"{\"title\":\"Total Synthesis of Eutyscoparol A and Violaceoid C\",\"authors\":\"\",\"doi\":\"10.1002/ajoc.202400148\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The total syntheses of eutyscoparol A and violaceoid C <em>via</em> violaceoid A, have been accomplished including the improved total syntheses of violaceoid A and violaceoid B. This synthetic method, which employed the desymmetrization of a symmetric diol, enabled divergent access to other violaceoids, eutyscoparols, and their derivatives.</p></div>\",\"PeriodicalId\":130,\"journal\":{\"name\":\"Asian Journal of Organic Chemistry\",\"volume\":\"13 7\",\"pages\":\"Article e202400148\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2024-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/ajoc.202400148\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Asian Journal of Organic Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2193580724001132\",\"RegionNum\":4,\"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":"Asian Journal of Organic Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2193580724001132","RegionNum":4,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, ORGANIC","Score":null,"Total":0}
引用次数: 0
摘要
我们完成了丁香油酚 A 的全合成和通过类中提琴酸 A 合成类中提琴酸 C 的全合成,包括改进了类中提琴酸 A 和类中提琴酸 B 的全合成。这种合成方法采用了不对称二元醇的非对称化技术,从而能够以不同的方法获得其他类长春花碱、丁香油醇及其衍生物。
Total Synthesis of Eutyscoparol A and Violaceoid C
The total syntheses of eutyscoparol A and violaceoid C via violaceoid A, have been accomplished including the improved total syntheses of violaceoid A and violaceoid B. This synthetic method, which employed the desymmetrization of a symmetric diol, enabled divergent access to other violaceoids, eutyscoparols, and their derivatives.
期刊介绍:
Organic chemistry is the fundamental science that stands at the heart of chemistry, biology, and materials science. Research in these areas is vigorous and truly international, with three major regions making almost equal contributions: America, Europe and Asia. Asia now has its own top international organic chemistry journal—the Asian Journal of Organic Chemistry (AsianJOC)
The AsianJOC is designed to be a top-ranked international research journal and publishes primary research as well as critical secondary information from authors across the world. The journal covers organic chemistry in its entirety. Authors and readers come from academia, the chemical industry, and government laboratories.