Different protocols (lithium enolate reactions, fluoride catalyzed and Lewis acid mediated silyl ketene acetal reactions) were studied to achieve stereoselectivity in the aldol reactions of \u3b3-thiobutyrolactone: in all cases benzaldehyde showed a striking peculiarity compared to aliphatic aldehydes
The aldol reaction plays an important role in organic synthesis and provides very useful synthetic t...
The origin of stereoselectivity in the reaction between a.-azido titanium enolate derived from chira...
International audiencePyruvate aldolases from Pfam family PF03328, recently described to be able to ...
A detailed Investigation of the enolization of phenyl thiopropionate with ethylenechloroboronate (EC...
BF3-OEt2 mediated thioester silylketene acetal additions to aldehydes are stereoconvergent and give ...
The stereochemical course of the aldol reaction has been studied with rationally designed and synthe...
The asymmetric aldol reaction of 1,2-diketones, masked as nonracemic 2-acyl dithiane oxides, with li...
Relative stereochemistry (chelation) effectively controls internal stereochemistry (syn-anti) in the...
The first organocatalytic, stereoselective and direct aldol reaction of activated thioesters with al...
A mannitol derived 2,3-butanediacetal ethyl ketone displays high levels of diastereoselectivity in b...
This review describes the use of catalytic asymmetric aldol reactions of silyl enol ethers and silyl...
Recoverable (S)-BINAM-L-prolinamide in combination with benzoic acid catalyzes and accelerates the ...
A versatile procedure for the gamma-vinylogous aldol reaction of the dioxinone-derived silyl enoleth...
The research summarized in this thesis focuses on synthesizing aldehyde and aldol compounds as subst...
Enolboronates, new enolates directly accessible from carbonyl compounds, exhibit extraordinary high ...
The aldol reaction plays an important role in organic synthesis and provides very useful synthetic t...
The origin of stereoselectivity in the reaction between a.-azido titanium enolate derived from chira...
International audiencePyruvate aldolases from Pfam family PF03328, recently described to be able to ...
A detailed Investigation of the enolization of phenyl thiopropionate with ethylenechloroboronate (EC...
BF3-OEt2 mediated thioester silylketene acetal additions to aldehydes are stereoconvergent and give ...
The stereochemical course of the aldol reaction has been studied with rationally designed and synthe...
The asymmetric aldol reaction of 1,2-diketones, masked as nonracemic 2-acyl dithiane oxides, with li...
Relative stereochemistry (chelation) effectively controls internal stereochemistry (syn-anti) in the...
The first organocatalytic, stereoselective and direct aldol reaction of activated thioesters with al...
A mannitol derived 2,3-butanediacetal ethyl ketone displays high levels of diastereoselectivity in b...
This review describes the use of catalytic asymmetric aldol reactions of silyl enol ethers and silyl...
Recoverable (S)-BINAM-L-prolinamide in combination with benzoic acid catalyzes and accelerates the ...
A versatile procedure for the gamma-vinylogous aldol reaction of the dioxinone-derived silyl enoleth...
The research summarized in this thesis focuses on synthesizing aldehyde and aldol compounds as subst...
Enolboronates, new enolates directly accessible from carbonyl compounds, exhibit extraordinary high ...
The aldol reaction plays an important role in organic synthesis and provides very useful synthetic t...
The origin of stereoselectivity in the reaction between a.-azido titanium enolate derived from chira...
International audiencePyruvate aldolases from Pfam family PF03328, recently described to be able to ...
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