Enantioselective bifunctional iminophosphorane catalyzed sulfa-Michael addition of alkyl thiols to unactivated β-substituted-α,β-unsaturated esters
The highly enantioselective sulfa-Michael addition of alkyl thiols to unactivated β-substituted-α,β-unsaturated esters catalyzed by a bifunctional iminophosphorane (BIMP) organocatalyst is described. The low acidity of the alkyl thiol pro-nucleophiles is overcome by the high Brønsted basicity of the...
Главные авторы: | Yang, J, Farley, A, Dixon, D |
---|---|
Формат: | Journal article |
Опубликовано: |
Royal Society of Chemistry
2016
|
Схожие документы
-
Bifunctional iminophosphorane-catalyzed enantioselective sulfa-michael addition to unactivated α,β-unsaturated amides
по: Rozsar, D, и др.
Опубликовано: (2022) -
Bifunctional iminophosphorane catalysed enantioselective sulfa-Michael addition of alkyl thiols to alkenyl benzimidazoles
по: Formica, M, и др.
Опубликовано: (2018) -
Bifunctional iminophosphorane-catalyzed enantioselective nitroalkane addition to unactivated α,β-unsaturated esters
по: Rozsar, D, и др.
Опубликовано: (2023) -
A bifunctional iminophosphorane squaramide catalyzed enantioselective synthesis of hydroquinazolines via intramolecular aza-Michael reaction to α,β-unsaturated esters
по: Su, G, и др.
Опубликовано: (2021) -
Bifunctional iminophosphorane catalyzed enantioselective ketimine phospha-Mannich reaction
по: Robertson, G, и др.
Опубликовано: (2015)