Reaction conditions have been identified to conduct a one-pot asymmetric organocatalytic aldol reaction with a hydrophobic substrate in aqueous medium via a process running in flow mode. By employing a mixture of water and 2-propanol, a hydrophobic aldehyde and 3.6 mol% of an organocatalyst, this microreactor process affords the desired aldol adduct with a conversion of 74% and an enantioselectivity of 89% after a reaction time of 60 minutes
none6noThe proline-catalysed asymmetric aldol reaction is usually carried out in highly dipolar apro...
Rulli G, Duangdee N, Hummel W, Berkessel A, Gröger H. First Tandem-Type One-Pot Process Combining As...
A novel C2-symmetrical bisprolinamide organocatalyst was synthesised and used to facilitate asymmetr...
Reaction conditions have been identified to conduct a one-pot asymmetric organocatalytic aldol react...
Reaction conditions have been identified to conduct a one-pot asymmetric organocatalytic aldol react...
Reaction conditions have been identified to conduct a one-pot asymmetric organocatalytic aldol react...
Reaction conditions have been identified to conduct a one-pot asymmetric organocatalytic aldol react...
\u3cp\u3eReaction conditions have been identified to conduct a one-pot asymmetric organocatalytic al...
Schober L, Ratnam S, Yamashita Y, et al. An Asymmetric Organocatalytic Aldol Reaction of a Hydrophob...
A rationally designed organocatalyst for direct asymmetric aldol reaction in the presence of water h...
A detailed study on the impact of the catalyst loading on conversion and enantioselectivity of the d...
Organocatalytic direct asymmetric anti-aldol reaction was developed in aqueous medium using a BINOL-...
The promiscuous aldo–ketoreductase (AKR) enzyme is used as a sustainable biocatalyst for the first t...
A suitable process window was identified for the combination of an asymmetric organocatalytic aldol ...
Asymmetric reactions in water and in aqueous solutions have become an area of fast growing interest ...
none6noThe proline-catalysed asymmetric aldol reaction is usually carried out in highly dipolar apro...
Rulli G, Duangdee N, Hummel W, Berkessel A, Gröger H. First Tandem-Type One-Pot Process Combining As...
A novel C2-symmetrical bisprolinamide organocatalyst was synthesised and used to facilitate asymmetr...
Reaction conditions have been identified to conduct a one-pot asymmetric organocatalytic aldol react...
Reaction conditions have been identified to conduct a one-pot asymmetric organocatalytic aldol react...
Reaction conditions have been identified to conduct a one-pot asymmetric organocatalytic aldol react...
Reaction conditions have been identified to conduct a one-pot asymmetric organocatalytic aldol react...
\u3cp\u3eReaction conditions have been identified to conduct a one-pot asymmetric organocatalytic al...
Schober L, Ratnam S, Yamashita Y, et al. An Asymmetric Organocatalytic Aldol Reaction of a Hydrophob...
A rationally designed organocatalyst for direct asymmetric aldol reaction in the presence of water h...
A detailed study on the impact of the catalyst loading on conversion and enantioselectivity of the d...
Organocatalytic direct asymmetric anti-aldol reaction was developed in aqueous medium using a BINOL-...
The promiscuous aldo–ketoreductase (AKR) enzyme is used as a sustainable biocatalyst for the first t...
A suitable process window was identified for the combination of an asymmetric organocatalytic aldol ...
Asymmetric reactions in water and in aqueous solutions have become an area of fast growing interest ...
none6noThe proline-catalysed asymmetric aldol reaction is usually carried out in highly dipolar apro...
Rulli G, Duangdee N, Hummel W, Berkessel A, Gröger H. First Tandem-Type One-Pot Process Combining As...
A novel C2-symmetrical bisprolinamide organocatalyst was synthesised and used to facilitate asymmetr...