C-Centred optically active allylsilanes react with carbonyl compounds in presence of Lewis acids to give the corresponding homoallyl alcohols with ee varying from 21 to 56 %. The role of the Lewis acid is crucial for a correct development of the reaction; different procedures are tested and the results compared. Allylsilanes carrying a chiral ligand react with carbonyl compounds and Lewis acids to give the corresponding homoallyl alcohols with ee varying from 21 to 56%
Chiral aryl methyl sulfoxides proved to be efficient activators in the asymmetric allylation of alde...
Asymmetric allylation of aldehydes with allyltrichlorosilane reagents, in recent years, has become a...
During investigations of cyclization reactions between chiral allylsilanes and N-acyliminium ions, i...
C-Centred optically active allylsilanes react with carbonyl compounds in presence of Lewis acids to ...
The use of chiral sulfoxides as Lewis base catalysts in the allylation of aldehydes with allyltrichl...
The chelating effect on regio- and stereochemical control of the homoallyl alcohol synthesis and ele...
The allylation of aldehydes is one of the most important methods for C-C bond formation because the ...
The allylation of aldehydes is one of the most important methods for C-C bond formation because the ...
The allylation of aldehydes is one of the most important methods for C-C bond formation because the ...
The allylation of aldehydes is one of the most important methods for C-C bond formation because the ...
Asymmetric allylation of aldehydes with allyltrichlorosilane reagents, in recent years, has become a...
The presence of a stereocenter close to the double bond of an allylsilane has an influence on the st...
The presence of a stereocenter close to the double bond of an allylsilane has an influence on the st...
The presence of a stereocenter close to the double bond of an allylsilane has an influence on the st...
Enantioselective organic catalysis represents one of the more rapidly expanding fields of research i...
Chiral aryl methyl sulfoxides proved to be efficient activators in the asymmetric allylation of alde...
Asymmetric allylation of aldehydes with allyltrichlorosilane reagents, in recent years, has become a...
During investigations of cyclization reactions between chiral allylsilanes and N-acyliminium ions, i...
C-Centred optically active allylsilanes react with carbonyl compounds in presence of Lewis acids to ...
The use of chiral sulfoxides as Lewis base catalysts in the allylation of aldehydes with allyltrichl...
The chelating effect on regio- and stereochemical control of the homoallyl alcohol synthesis and ele...
The allylation of aldehydes is one of the most important methods for C-C bond formation because the ...
The allylation of aldehydes is one of the most important methods for C-C bond formation because the ...
The allylation of aldehydes is one of the most important methods for C-C bond formation because the ...
The allylation of aldehydes is one of the most important methods for C-C bond formation because the ...
Asymmetric allylation of aldehydes with allyltrichlorosilane reagents, in recent years, has become a...
The presence of a stereocenter close to the double bond of an allylsilane has an influence on the st...
The presence of a stereocenter close to the double bond of an allylsilane has an influence on the st...
The presence of a stereocenter close to the double bond of an allylsilane has an influence on the st...
Enantioselective organic catalysis represents one of the more rapidly expanding fields of research i...
Chiral aryl methyl sulfoxides proved to be efficient activators in the asymmetric allylation of alde...
Asymmetric allylation of aldehydes with allyltrichlorosilane reagents, in recent years, has become a...
During investigations of cyclization reactions between chiral allylsilanes and N-acyliminium ions, i...