{"title":"taddol锂-三乙基硼体系催化丙二酸酯与查尔酮的Michael加成反应。","authors":"J Irurre, M Riera, C Amela-Cortés","doi":"","DOIUrl":null,"url":null,"abstract":"<p><p>The reaction mixture obtained by treating equimolar amounts of a TADDOL with lithium triethylborohydride promotes the catalytic enantioselective Michael addition of malonates to chalcone with good yields and moderate enantioselectivities. The catalyst is alternatively generated reacting the 1,4-diol with butyllithium and triethylborane. The adduct of dibenzyl malonate to chalcone is attained with 99% ee, after one recrystallization. The reaction scale-up was achieved successfully.</p>","PeriodicalId":11752,"journal":{"name":"Enantiomer","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2000-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Lithium TADDOLate-triethylboron system as a promoter for the catalytic enantioselective Michael addition of malonates to chalcone.\",\"authors\":\"J Irurre, M Riera, C Amela-Cortés\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The reaction mixture obtained by treating equimolar amounts of a TADDOL with lithium triethylborohydride promotes the catalytic enantioselective Michael addition of malonates to chalcone with good yields and moderate enantioselectivities. The catalyst is alternatively generated reacting the 1,4-diol with butyllithium and triethylborane. The adduct of dibenzyl malonate to chalcone is attained with 99% ee, after one recrystallization. The reaction scale-up was achieved successfully.</p>\",\"PeriodicalId\":11752,\"journal\":{\"name\":\"Enantiomer\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2000-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Enantiomer\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Enantiomer","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Lithium TADDOLate-triethylboron system as a promoter for the catalytic enantioselective Michael addition of malonates to chalcone.
The reaction mixture obtained by treating equimolar amounts of a TADDOL with lithium triethylborohydride promotes the catalytic enantioselective Michael addition of malonates to chalcone with good yields and moderate enantioselectivities. The catalyst is alternatively generated reacting the 1,4-diol with butyllithium and triethylborane. The adduct of dibenzyl malonate to chalcone is attained with 99% ee, after one recrystallization. The reaction scale-up was achieved successfully.