{"title":"叔丁醇锂介导的无保护的吲哚和吡咯与二氧化碳的羧基化反应(在Kuwajima教授77岁生日之际献给他)","authors":"Woo‐Jin Yoo, Thanh V. Q. Nguyen, M. Capdevila","doi":"10.1002/CHIN.201520133","DOIUrl":null,"url":null,"abstract":"The base-mediated and transition metal-free carboxylation reaction smoothly proceeds under ambient pressure of carbon dioxide with the use of a large excess of LiOtBu.","PeriodicalId":12850,"journal":{"name":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2015-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"LITHIUM tert-BUTOXIDE-MEDIATED CARBOXYLATION REACTIONS OF UNPROTECTED INDOLES AND PYRROLES WITH CARBON DIOXIDE (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)\",\"authors\":\"Woo‐Jin Yoo, Thanh V. Q. Nguyen, M. Capdevila\",\"doi\":\"10.1002/CHIN.201520133\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The base-mediated and transition metal-free carboxylation reaction smoothly proceeds under ambient pressure of carbon dioxide with the use of a large excess of LiOtBu.\",\"PeriodicalId\":12850,\"journal\":{\"name\":\"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2015-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1002/CHIN.201520133\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Heterocycles : an international journal for reviews and communications in heterocyclic chemistry","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1002/CHIN.201520133","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
LITHIUM tert-BUTOXIDE-MEDIATED CARBOXYLATION REACTIONS OF UNPROTECTED INDOLES AND PYRROLES WITH CARBON DIOXIDE (Dedicated to Professor Isao Kuwajima on the occasion of his 77th birthday)
The base-mediated and transition metal-free carboxylation reaction smoothly proceeds under ambient pressure of carbon dioxide with the use of a large excess of LiOtBu.
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