{"title":"n -碘琥珀酰亚胺或分子碘影响下2-烯丙基-1-萘酚的区域选择性5-外三角杂环化","authors":"P. K. Basu, Amrita Ghosh","doi":"10.1155/2012/810476","DOIUrl":null,"url":null,"abstract":"Regioselective iodocyclization of a series of allylhydroxy naphthalene precursors involving N-iodosuccinimide and environment friendly green approach associated with surfactant-promoted molecular-iodine-mediated 5-exo-trig cyclization strategies has been explored.","PeriodicalId":19688,"journal":{"name":"Organic Chemistry International","volume":"27 1","pages":"1-7"},"PeriodicalIF":0.0000,"publicationDate":"2012-11-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Regioselective 5-exo-Trig Heterocyclization of 2-Allyl-1-naphthols under the Influence of N-Iodosuccinimide or Molecular Iodine in Aqueous Micelle\",\"authors\":\"P. K. Basu, Amrita Ghosh\",\"doi\":\"10.1155/2012/810476\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Regioselective iodocyclization of a series of allylhydroxy naphthalene precursors involving N-iodosuccinimide and environment friendly green approach associated with surfactant-promoted molecular-iodine-mediated 5-exo-trig cyclization strategies has been explored.\",\"PeriodicalId\":19688,\"journal\":{\"name\":\"Organic Chemistry International\",\"volume\":\"27 1\",\"pages\":\"1-7\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2012-11-22\",\"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/10.1155/2012/810476\",\"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/10.1155/2012/810476","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Regioselective 5-exo-Trig Heterocyclization of 2-Allyl-1-naphthols under the Influence of N-Iodosuccinimide or Molecular Iodine in Aqueous Micelle
Regioselective iodocyclization of a series of allylhydroxy naphthalene precursors involving N-iodosuccinimide and environment friendly green approach associated with surfactant-promoted molecular-iodine-mediated 5-exo-trig cyclization strategies has been explored.
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