This paper describes the use of bifunctional thiourea catalysts in the intramolecular reaction of a nitronate with conjugated ketones to generate the corresponding γ-nitroketones. In contrast to our previous studies in this area, we obtained the cis-functionalized systems as the major diastereoisomers in good yields and reasonable selectivities
he combination of small-molecule catalysis and enzyme catalysis represents an underexploited area of...
he combination of small-molecule catalysis and enzyme catalysis represents an underexploited area of...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
I. Enantio- and Diastereoselective Organocatalytic Conjugate Additions of Nitroalkanes to Enone Dies...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
An organocatalytic asymmetric synthesis of a novel, highly functionalised cyclopropane system furnis...
The conjugate addition of nitroalkanes to electron-poor alkenes is a widely used process which only ...
The asymmetric conjugate addition of carbon and heteroatom nucleophiles to nitroalkenes is a very in...
Natural products are the source of many valuable folk medicines and pharmaceutical agents. However, ...
This thesis is concerned with the design, synthesis and use of novel bifunctional organocatalysts fo...
Enantiomerically pure carbamate-monoprotected trans-cyclohexane-1,2-diamines are used as chiral orga...
This thesis is concerned with the design, synthesis and use of novel bifunctional organocatalysts fo...
he combination of small-molecule catalysis and enzyme catalysis represents an underexploited area of...
he combination of small-molecule catalysis and enzyme catalysis represents an underexploited area of...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
I. Enantio- and Diastereoselective Organocatalytic Conjugate Additions of Nitroalkanes to Enone Dies...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
International audienceA new method has been developed for the enantioselective synthesis of highly f...
An organocatalytic asymmetric synthesis of a novel, highly functionalised cyclopropane system furnis...
The conjugate addition of nitroalkanes to electron-poor alkenes is a widely used process which only ...
The asymmetric conjugate addition of carbon and heteroatom nucleophiles to nitroalkenes is a very in...
Natural products are the source of many valuable folk medicines and pharmaceutical agents. However, ...
This thesis is concerned with the design, synthesis and use of novel bifunctional organocatalysts fo...
Enantiomerically pure carbamate-monoprotected trans-cyclohexane-1,2-diamines are used as chiral orga...
This thesis is concerned with the design, synthesis and use of novel bifunctional organocatalysts fo...
he combination of small-molecule catalysis and enzyme catalysis represents an underexploited area of...
he combination of small-molecule catalysis and enzyme catalysis represents an underexploited area of...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...