Thi Minh Thi Le, Mingbing Zhong, P. Jubault, T. Poisson
{"title":"铜催化化学选择性硝基还原","authors":"Thi Minh Thi Le, Mingbing Zhong, P. Jubault, T. Poisson","doi":"10.1055/a-2326-6363","DOIUrl":null,"url":null,"abstract":"The reduction of nitro compounds into the highly valuable anilines was reported using a Cu-catalyst and B2Pin2. The reaction proceeded under very mild reaction conditions and showcased an excellent functional group tolerance. This method was applied to a large panel of nitro derivatives including biorelevant molecules and important synthetic intermediates toward the synthesis of API. This novel reaction manifold intends to provide a complementary approach to the existing portfolio of nitro-reduction methods.","PeriodicalId":510101,"journal":{"name":"Synthesis","volume":"21 3","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Copper Catalyzed Chemoselective Nitro Reduction\",\"authors\":\"Thi Minh Thi Le, Mingbing Zhong, P. Jubault, T. Poisson\",\"doi\":\"10.1055/a-2326-6363\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"The reduction of nitro compounds into the highly valuable anilines was reported using a Cu-catalyst and B2Pin2. The reaction proceeded under very mild reaction conditions and showcased an excellent functional group tolerance. This method was applied to a large panel of nitro derivatives including biorelevant molecules and important synthetic intermediates toward the synthesis of API. This novel reaction manifold intends to provide a complementary approach to the existing portfolio of nitro-reduction methods.\",\"PeriodicalId\":510101,\"journal\":{\"name\":\"Synthesis\",\"volume\":\"21 3\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-05-14\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Synthesis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1055/a-2326-6363\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Synthesis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1055/a-2326-6363","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The reduction of nitro compounds into the highly valuable anilines was reported using a Cu-catalyst and B2Pin2. The reaction proceeded under very mild reaction conditions and showcased an excellent functional group tolerance. This method was applied to a large panel of nitro derivatives including biorelevant molecules and important synthetic intermediates toward the synthesis of API. This novel reaction manifold intends to provide a complementary approach to the existing portfolio of nitro-reduction methods.