Miguel Angel González Cardente, Stuart McCulloch, Gerald Pattenden
{"title":"级联自由基介导的雌激素类固醇大环化-环化途径","authors":"Miguel Angel González Cardente, Stuart McCulloch, Gerald Pattenden","doi":"10.1016/S1387-1609(01)01271-3","DOIUrl":null,"url":null,"abstract":"<div><p>A new approach to ring A aromatic steroids, based on cascade 13-<em>endo</em>-<em>trig/dig</em> macrocyclisations followed by sequential 5-<em>exo-trig</em> and 6-<em>exo-trig</em> transannulations, exemplified in the syntheses of the <em>cis,anti,trans</em> tetracycle <strong>9</strong> and the <em>trans,syn</em> tetracycle <strong>13</strong> from the <em>ortho</em>-substituted aryl polyen(yne) precursors, <strong>8</strong> and <strong>12</strong> respectively, is described.</p></div>","PeriodicalId":100305,"journal":{"name":"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry","volume":"4 7","pages":"Pages 571-574"},"PeriodicalIF":0.0000,"publicationDate":"2001-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/S1387-1609(01)01271-3","citationCount":"0","resultStr":"{\"title\":\"A cascade radical-mediated macrocyclisation–transannulation approach to oestrogen steroids\",\"authors\":\"Miguel Angel González Cardente, Stuart McCulloch, Gerald Pattenden\",\"doi\":\"10.1016/S1387-1609(01)01271-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>A new approach to ring A aromatic steroids, based on cascade 13-<em>endo</em>-<em>trig/dig</em> macrocyclisations followed by sequential 5-<em>exo-trig</em> and 6-<em>exo-trig</em> transannulations, exemplified in the syntheses of the <em>cis,anti,trans</em> tetracycle <strong>9</strong> and the <em>trans,syn</em> tetracycle <strong>13</strong> from the <em>ortho</em>-substituted aryl polyen(yne) precursors, <strong>8</strong> and <strong>12</strong> respectively, is described.</p></div>\",\"PeriodicalId\":100305,\"journal\":{\"name\":\"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry\",\"volume\":\"4 7\",\"pages\":\"Pages 571-574\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2001-07-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/S1387-1609(01)01271-3\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1387160901012713\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Comptes Rendus de l'Académie des Sciences - Series IIC - Chemistry","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1387160901012713","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
A cascade radical-mediated macrocyclisation–transannulation approach to oestrogen steroids
A new approach to ring A aromatic steroids, based on cascade 13-endo-trig/dig macrocyclisations followed by sequential 5-exo-trig and 6-exo-trig transannulations, exemplified in the syntheses of the cis,anti,trans tetracycle 9 and the trans,syn tetracycle 13 from the ortho-substituted aryl polyen(yne) precursors, 8 and 12 respectively, is described.