{"title":"分子内流动光化学 [2+2] 环加成法桥式双环 gamma-Sultams","authors":"Oleksandr, Grygorenko, Yevhen, Zaika, Illia, Borodin, Heorhii, Olekh, Maksym, Kovalov, Oleksandr, Diachenko, Volodymyr, Brovarets, Bohdan, Vashchenko","doi":"10.26434/chemrxiv-2024-wcxr0","DOIUrl":null,"url":null,"abstract":"An elegant synthetic approach to the construction of a novel saturated heterocycle – 2-thia-3-azabicyclo[2.1.1]hexane 2,2-dioxide – was designed. The key step included intramolecular flow photochemical [2 + 2] cycloaddition of appropriately substituted dienes, in turn obtained from readily available starting materials on a multigram scale. Further synthetic transformations of the resulting bicyclic compounds enabled the preparation of numerous functionalized derivatives useful for early drug discovery programs as promising isosteres of pyrrolidine, pyrrolidone, and gamma-sultams, and also demonstrated tolerance of the title bicyclic system towards typical organic chemistry reaction conditions.","PeriodicalId":9813,"journal":{"name":"ChemRxiv","volume":"18 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-09-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Bridged Bicyclic gamma-Sultams by Intramolecular Flow Photochemical [2+2] Cycloaddition\",\"authors\":\"Oleksandr, Grygorenko, Yevhen, Zaika, Illia, Borodin, Heorhii, Olekh, Maksym, Kovalov, Oleksandr, Diachenko, Volodymyr, Brovarets, Bohdan, Vashchenko\",\"doi\":\"10.26434/chemrxiv-2024-wcxr0\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An elegant synthetic approach to the construction of a novel saturated heterocycle – 2-thia-3-azabicyclo[2.1.1]hexane 2,2-dioxide – was designed. The key step included intramolecular flow photochemical [2 + 2] cycloaddition of appropriately substituted dienes, in turn obtained from readily available starting materials on a multigram scale. Further synthetic transformations of the resulting bicyclic compounds enabled the preparation of numerous functionalized derivatives useful for early drug discovery programs as promising isosteres of pyrrolidine, pyrrolidone, and gamma-sultams, and also demonstrated tolerance of the title bicyclic system towards typical organic chemistry reaction conditions.\",\"PeriodicalId\":9813,\"journal\":{\"name\":\"ChemRxiv\",\"volume\":\"18 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ChemRxiv\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.26434/chemrxiv-2024-wcxr0\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ChemRxiv","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.26434/chemrxiv-2024-wcxr0","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Bridged Bicyclic gamma-Sultams by Intramolecular Flow Photochemical [2+2] Cycloaddition
An elegant synthetic approach to the construction of a novel saturated heterocycle – 2-thia-3-azabicyclo[2.1.1]hexane 2,2-dioxide – was designed. The key step included intramolecular flow photochemical [2 + 2] cycloaddition of appropriately substituted dienes, in turn obtained from readily available starting materials on a multigram scale. Further synthetic transformations of the resulting bicyclic compounds enabled the preparation of numerous functionalized derivatives useful for early drug discovery programs as promising isosteres of pyrrolidine, pyrrolidone, and gamma-sultams, and also demonstrated tolerance of the title bicyclic system towards typical organic chemistry reaction conditions.