Naturally synthetic: Acid/base catalyst (S)‐1 can be used in highly enantioselective alcoholytic desymmetrizations of meso anhydrides. For example, the methanolysis of cyclobutane anhydride derivative 2 gave hemiester 3 in 99:1 e.r. (see scheme). Ester 3 was used in a short enantioselective synthesis of (+)‐grandisol
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
The alcoholysis of cyclic meso-anhydrides catalyzed by β-amino alcohols has been investigated with D...
Establishing one-pot, multi-step protocols combining different types of catalysts is one important g...
The enantioselective desymmetrization is regarded as an effective strategy for producing chiral comp...
The enantioselective desymmetrization is regarded as an effective strategy for producing chiral comp...
The enantioselective desymmetrization is regarded as an effective strategy for producing chiral comp...
A family of novel chloramphenicol base-amide organocatalysts possessing a NH functionality at C-1 po...
Cycloaddition reactions between enolisable anhydrides and imines have long been known as excellent t...
This study describes an organocatalytic kinetic resolution of racemic secondary nitroallylic alcohol...
International audienceSynthesis of biologically active molecules (whether at laboratory or industria...
Bicyclic succinic anhydrides alkylated at the <i>α</i>-position have been prepared and submitted to ...
The synthesis of enantiomerically pure compounds is of vital importance. Most biologically active na...
The synthesis of enantiomerically pure compounds is of vital importance. Most biologically active na...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
This thesis describes new chiral Brønsted acid catalyzed asymmetric reactions of alcohol pro-electro...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
The alcoholysis of cyclic meso-anhydrides catalyzed by β-amino alcohols has been investigated with D...
Establishing one-pot, multi-step protocols combining different types of catalysts is one important g...
The enantioselective desymmetrization is regarded as an effective strategy for producing chiral comp...
The enantioselective desymmetrization is regarded as an effective strategy for producing chiral comp...
The enantioselective desymmetrization is regarded as an effective strategy for producing chiral comp...
A family of novel chloramphenicol base-amide organocatalysts possessing a NH functionality at C-1 po...
Cycloaddition reactions between enolisable anhydrides and imines have long been known as excellent t...
This study describes an organocatalytic kinetic resolution of racemic secondary nitroallylic alcohol...
International audienceSynthesis of biologically active molecules (whether at laboratory or industria...
Bicyclic succinic anhydrides alkylated at the <i>α</i>-position have been prepared and submitted to ...
The synthesis of enantiomerically pure compounds is of vital importance. Most biologically active na...
The synthesis of enantiomerically pure compounds is of vital importance. Most biologically active na...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
This thesis describes new chiral Brønsted acid catalyzed asymmetric reactions of alcohol pro-electro...
A novel bifunctional catalyst derived from BINOL has been developed that promotes the highly enantio...
The alcoholysis of cyclic meso-anhydrides catalyzed by β-amino alcohols has been investigated with D...
Establishing one-pot, multi-step protocols combining different types of catalysts is one important g...
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