{"title":"电化学钴催化的芳基膦酰胺与羧酸的对映选择性 C-H 乙酰氧基化反应","authors":"","doi":"10.1039/d4gc01404a","DOIUrl":null,"url":null,"abstract":"<div><p>We presented a first example of cobalt-electro-catalyzed enantioselective C–H acyloxylation of arylphosphinamides with carboxylic acids, enabling the concise synthesis of oxygenated phosphamides featuring a P-stereogenic center. These compounds were synthesized with acceptable yields and outstanding enantioselectivities. The reaction demonstrated a broad substrate scope and good functional group tolerance. Additionally, the facile conversion of the acyloxy group to a free hydroxyl group provides opportunities for further chemical manipulations, underscoring the versatility of this strategy.</p></div>","PeriodicalId":78,"journal":{"name":"Green Chemistry","volume":null,"pages":null},"PeriodicalIF":9.3000,"publicationDate":"2024-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Electrochemically enabled cobalt catalyzed enantioselective C–H acyloxylation of aryl phosphamide with carboxylic acid†\",\"authors\":\"\",\"doi\":\"10.1039/d4gc01404a\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>We presented a first example of cobalt-electro-catalyzed enantioselective C–H acyloxylation of arylphosphinamides with carboxylic acids, enabling the concise synthesis of oxygenated phosphamides featuring a P-stereogenic center. These compounds were synthesized with acceptable yields and outstanding enantioselectivities. The reaction demonstrated a broad substrate scope and good functional group tolerance. Additionally, the facile conversion of the acyloxy group to a free hydroxyl group provides opportunities for further chemical manipulations, underscoring the versatility of this strategy.</p></div>\",\"PeriodicalId\":78,\"journal\":{\"name\":\"Green Chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":9.3000,\"publicationDate\":\"2024-07-15\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Green Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S1463926224006241\",\"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":"Green Chemistry","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S1463926224006241","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
Electrochemically enabled cobalt catalyzed enantioselective C–H acyloxylation of aryl phosphamide with carboxylic acid†
We presented a first example of cobalt-electro-catalyzed enantioselective C–H acyloxylation of arylphosphinamides with carboxylic acids, enabling the concise synthesis of oxygenated phosphamides featuring a P-stereogenic center. These compounds were synthesized with acceptable yields and outstanding enantioselectivities. The reaction demonstrated a broad substrate scope and good functional group tolerance. Additionally, the facile conversion of the acyloxy group to a free hydroxyl group provides opportunities for further chemical manipulations, underscoring the versatility of this strategy.
期刊介绍:
Green Chemistry is a journal that provides a unique forum for the publication of innovative research on the development of alternative green and sustainable technologies. The scope of Green Chemistry is based on the definition proposed by Anastas and Warner (Green Chemistry: Theory and Practice, P T Anastas and J C Warner, Oxford University Press, Oxford, 1998), which defines green chemistry as the utilisation of a set of principles that reduces or eliminates the use or generation of hazardous substances in the design, manufacture and application of chemical products. Green Chemistry aims to reduce the environmental impact of the chemical enterprise by developing a technology base that is inherently non-toxic to living things and the environment. The journal welcomes submissions on all aspects of research relating to this endeavor and publishes original and significant cutting-edge research that is likely to be of wide general appeal. For a work to be published, it must present a significant advance in green chemistry, including a comparison with existing methods and a demonstration of advantages over those methods.