脱氢松香胺-辛可宁-方酰胺催化的2,4-戊二酮对硝基烯的不对称迈克加成反应
Enantioselective Michael addition of 2,4-pentanedione To nitroalkenes catalyzed by dehydroabietylamine-cinchonine-squaramide
在这篇文章中,基于天然松香衍生物的特殊活性和方酰胺有机催化剂的良好的不对称诱导活性,一种新型的脱氢松香胺-辛可宁-方酰胺有机催化剂被应用于2,4-戊二酮对硝基烯烃的不对称迈克加成反应中。研究发现,在5 mol%催化量的脱氢松香胺-辛可宁-方酰胺有机催化剂的存在下,可有效实现2,4-戊二酮对硝基烯烃的不对称加成反应,得到系列具有光学活性的硝基衍生物,产物的产率高达99%,产物的对映选择性高达89%。
In this paper, on the basis of the special activity of natural rosin derivatives and the good asymmetric induction activity of squaramide organic catalysts, a novel dehydroabietylamine-cinchonine-squaramide catalyst has been developed for asymmetric Michael addition of 2,4-pentanedione to nitroalkenes. It found that with using 5 mol% dehydroabietylamine-cinchonine-squaramide catalyst , the reaction of 2,4-pentanedione to nitroalkenes could act effectively, and a series of nitroalkene derivatives possessing optical activity were afforded with high reaction yields and excellent enantioselectivities (up to 99% yield, 89% ee).
彭雪珂、郑杰、董春娥
有机化学工业精细化学工业
有机化学脱氢松香胺-辛可宁-方酰胺不对称迈克加成反应硝基烯
Organic chemistryDehydroabietylamine-cinchonine-squaramideMichael additionNitroalkenes
彭雪珂,郑杰,董春娥.脱氢松香胺-辛可宁-方酰胺催化的2,4-戊二酮对硝基烯的不对称迈克加成反应[EB/OL].(2018-04-18)[2025-08-16].http://www.paper.edu.cn/releasepaper/content/201804-172.点此复制
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