{"title":"取代5-羟基硫代-7h-硫代[3,2-g][1]苯并噻吩吡喃-7-ones的简易合成","authors":"G. Chandramouli, P. Reddy, B. Prassana","doi":"10.1080/0278611021000011965","DOIUrl":null,"url":null,"abstract":"Lewis acid (BF 3 (OEt) 2 ) in dry diethyl ether mediated cyclization and demethylation of substituted 2-(2-methyl-3-methylsulfanyl-phenylsulfanyl)-1,2-diphenyl-ethanones (3a-e) at ambient temperature gave 7-methyl-2,3-diphenyl-6-thio-benzo[b]thiophenes (4a-e). Treatment of (4a-e) with substituted malonic acids furnishes the corresponding substituted 5-hydroxythio-7H-thieno[3,2-g][1] benzothiopyran-7-aones. These were characterized by their elemental, IR, 1 H NMR and mass spectral analysis.","PeriodicalId":22122,"journal":{"name":"Sulfur Letters","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2003-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Facile synthesis of substituted 5-hydroxythio-7h-thieno[3,2-g] [1]benzothiopyran-7-ones\",\"authors\":\"G. Chandramouli, P. Reddy, B. Prassana\",\"doi\":\"10.1080/0278611021000011965\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Lewis acid (BF 3 (OEt) 2 ) in dry diethyl ether mediated cyclization and demethylation of substituted 2-(2-methyl-3-methylsulfanyl-phenylsulfanyl)-1,2-diphenyl-ethanones (3a-e) at ambient temperature gave 7-methyl-2,3-diphenyl-6-thio-benzo[b]thiophenes (4a-e). Treatment of (4a-e) with substituted malonic acids furnishes the corresponding substituted 5-hydroxythio-7H-thieno[3,2-g][1] benzothiopyran-7-aones. These were characterized by their elemental, IR, 1 H NMR and mass spectral analysis.\",\"PeriodicalId\":22122,\"journal\":{\"name\":\"Sulfur Letters\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2003-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sulfur Letters\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1080/0278611021000011965\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sulfur Letters","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1080/0278611021000011965","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Facile synthesis of substituted 5-hydroxythio-7h-thieno[3,2-g] [1]benzothiopyran-7-ones
Lewis acid (BF 3 (OEt) 2 ) in dry diethyl ether mediated cyclization and demethylation of substituted 2-(2-methyl-3-methylsulfanyl-phenylsulfanyl)-1,2-diphenyl-ethanones (3a-e) at ambient temperature gave 7-methyl-2,3-diphenyl-6-thio-benzo[b]thiophenes (4a-e). Treatment of (4a-e) with substituted malonic acids furnishes the corresponding substituted 5-hydroxythio-7H-thieno[3,2-g][1] benzothiopyran-7-aones. These were characterized by their elemental, IR, 1 H NMR and mass spectral analysis.
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