A novel isosteviol‐based bifunctional squaramide organocatalyst for enantioselective Michael addition of acetylacetone to nitroolefins

التفاصيل البيبلوغرافية
العنوان: A novel isosteviol‐based bifunctional squaramide organocatalyst for enantioselective Michael addition of acetylacetone to nitroolefins
المؤلفون: Jing-Chao Tao, Xiaopei Chen, Quanjian Lv, Zhijing Liu, Zhi-Wei Ma, Chuanchuan Wang
المصدر: Chirality. 34:77-85
بيانات النشر: Wiley, 2021.
سنة النشر: 2021
مصطلحات موضوعية: Pharmacology, Quinine, Acetylacetone, Organic Chemistry, Enantioselective synthesis, Squaramide, Stereoisomerism, Alkenes, Combinatorial chemistry, Catalysis, Analytical Chemistry, Bifunctional catalyst, chemistry.chemical_compound, chemistry, Pentanones, Organocatalysis, Drug Discovery, Michael reaction, Stevioside, Diterpenes, Kaurane, Bifunctional, Spectroscopy
الوصف: Chiral amine-squaramide is a kind of effective hydrogen bond donor bifunctional catalyst to promote many asymmetric transformations. In this paper, novel chiral tertiary amine-squaramide derived from the natural product of the stevioside was developed and applied into the asymmetric Michael addition of acetylacetone to nitroolefins. This asymmetric reaction performed well, and a series of enantiomerically enriched compounds were obtained in high yields (up to 96%) with excellent enantioselectivities (up to 99% ee).
تدمد: 1520-636X
0899-0042
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9844110e93b21c3adbb06de65e62092a
https://doi.org/10.1002/chir.23391
حقوق: CLOSED
رقم الأكسشن: edsair.doi.dedup.....9844110e93b21c3adbb06de65e62092a
قاعدة البيانات: OpenAIRE