Chiranjeevi Korupalli, Arpan Dandapat, D. Prasad, G. Sekar
{"title":"铜(I)-二醇通过()-O键形成催化1,4-苯并恶硫汀的多米诺合成","authors":"Chiranjeevi Korupalli, Arpan Dandapat, D. Prasad, G. Sekar","doi":"10.1155/2011/980765","DOIUrl":null,"url":null,"abstract":"1,4-benzoxathiine moieties can be synthesized by domino SN2 ring opening of epoxide with o-halothiophenols followed by the copper(I)-BINOL catalyzed Ullmann-type coupling cyclization (intramolecular C(aryl)-O bond formation) with moderate to good yields.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"30 1","pages":"1-7"},"PeriodicalIF":0.0000,"publicationDate":"2011-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Copper(I)-BINOL Catalyzed Domino Synthesis of 1,4-Benzoxathiines through ()-O Bond Formation\",\"authors\":\"Chiranjeevi Korupalli, Arpan Dandapat, D. Prasad, G. Sekar\",\"doi\":\"10.1155/2011/980765\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"1,4-benzoxathiine moieties can be synthesized by domino SN2 ring opening of epoxide with o-halothiophenols followed by the copper(I)-BINOL catalyzed Ullmann-type coupling cyclization (intramolecular C(aryl)-O bond formation) with moderate to good yields.\",\"PeriodicalId\":19688,\"journal\":{\"name\":\"Organic Chemistry International\",\"volume\":\"30 1\",\"pages\":\"1-7\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2011-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organic Chemistry International\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1155/2011/980765\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organic Chemistry International","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/2011/980765","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Copper(I)-BINOL Catalyzed Domino Synthesis of 1,4-Benzoxathiines through ()-O Bond Formation
1,4-benzoxathiine moieties can be synthesized by domino SN2 ring opening of epoxide with o-halothiophenols followed by the copper(I)-BINOL catalyzed Ullmann-type coupling cyclization (intramolecular C(aryl)-O bond formation) with moderate to good yields.