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2014 | 12 | 3 | 416-425
Tytuł artykułu

Enantioselective Michael additions of aldehydes to nitroalkenes catalyzed with ionically tagged organocatalyst

Treść / Zawartość
Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Enantioselective organocatalytic Michael additions affords useful building blocks for many biologically and medicinally relevant compounds. Ionically-tagged diphenylprolinol silyl ether efficiently catalyzes several Michael additions of aldehydes to nitroalkenes in ionic liquids. The Michael additions work well in ionic liquids; yields up to 95% and enantioselectivities up to 95% ee were achieved. Furthermore, in some cases, the catalytic system was reusable.
Wydawca

Czasopismo
Rocznik
Tom
12
Numer
3
Strony
416-425
Opis fizyczny
Daty
wydano
2014-03-01
online
2013-12-21
Twórcy
  • Synkola
Bibliografia
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Typ dokumentu
Bibliografia
Identyfikatory
Identyfikator YADDA
bwmeta1.element.-psjd-doi-10_2478_s11532-013-0391-4
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