A novel calix[4]arene-based bifunctional squaramide organocatalyst for enantioselective Michael addition of acetylacetone to nitroolefins
Küçük Resim Yok
Tarih
2016
Yazarlar
Dergi Başlığı
Dergi ISSN
Cilt Başlığı
Yayıncı
Royal Soc Chemistry
Erişim Hakkı
info:eu-repo/semantics/closedAccess
Özet
A new chiral calix[4]arene-based organocatalyst 3 bearing bis-squaramide moieties was designed and synthesized from p-tert-butylcalix[4] arene. This bifunctional squaramide organocatalyst was used in the enantioselective conjugate addition of acetylacetone to beta-nitrostyrenes. The corresponding adducts were obtained in good to excellent yields with high enantioselectivities (up to 94% ee).
Açıklama
Anahtar Kelimeler
[Keyword Not Available]
Kaynak
Organic Chemistry Frontiers
WoS Q Değeri
Q1
Scopus Q Değeri
Q1
Cilt
3
Sayı
6