Our interest in the synthesis of compact nitrogen heterocycles from abundant sources has motivated a critical analysis of the status in azomethine ylide chemistry. Despite the outstanding developments in catalytic enantioselective [3+2] cycloadditions, these are still limited to electron-poor olefins. Only a few examples can be found in the literature that report on cycloadditions using non-electrophilic alkenes and those are compiled herein. With this account we aim to extract lessons and challenges that will inspire future breakthroughs in this area
The thermal 1,3-dipolar cycloaddition of unactivated azomethine ylides derived from allylamine and a...
Catalytic enantioselective tandem carbonyl ylide formation-cycloaddition reactions of tert-butyl 2-d...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
Our interest in the synthesis of compact nitrogen heterocycles from abundant sources has motivated a...
The reaction of azomethine ylide 1,3-dipoles with olefinic dipo-larophiles forms highly substituted ...
CONSPECTUS: Cycloaddition reactions are among the most powerful methods for the synthesis of complex...
The intermolecular 1,3-dipolar cycloaddition reaction of azomethine ylides with carbon-carbon double...
International audienceNon-stabilized azomethine ylide 4a reacts smoothly at room temperature with a ...
A general strategy for the construction of X-azabicyclo[m.2.1]alkane frameworks in optically pure fo...
Various new structural entities related to x-azatricyclo[m.n.0.0a,b]alkanes are constructed by the i...
Deprotonation of trifluoromethyl or cyano thioamidium salts generates new azomethine ylides which un...
ABSTRACT: The first examples of azomethine ylides derived from allylic amine and glyoxal precursors ...
This review summarizes the trends in the formation of complex or not so complex heterocyclic structu...
The research on azomethine ylide 1,3-dipoles, developed in the last five years in the Institute of A...
Conjugated cyclic trienes without nonbenzenoid aromatic characteristic were successfully employed as...
The thermal 1,3-dipolar cycloaddition of unactivated azomethine ylides derived from allylamine and a...
Catalytic enantioselective tandem carbonyl ylide formation-cycloaddition reactions of tert-butyl 2-d...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
Our interest in the synthesis of compact nitrogen heterocycles from abundant sources has motivated a...
The reaction of azomethine ylide 1,3-dipoles with olefinic dipo-larophiles forms highly substituted ...
CONSPECTUS: Cycloaddition reactions are among the most powerful methods for the synthesis of complex...
The intermolecular 1,3-dipolar cycloaddition reaction of azomethine ylides with carbon-carbon double...
International audienceNon-stabilized azomethine ylide 4a reacts smoothly at room temperature with a ...
A general strategy for the construction of X-azabicyclo[m.2.1]alkane frameworks in optically pure fo...
Various new structural entities related to x-azatricyclo[m.n.0.0a,b]alkanes are constructed by the i...
Deprotonation of trifluoromethyl or cyano thioamidium salts generates new azomethine ylides which un...
ABSTRACT: The first examples of azomethine ylides derived from allylic amine and glyoxal precursors ...
This review summarizes the trends in the formation of complex or not so complex heterocyclic structu...
The research on azomethine ylide 1,3-dipoles, developed in the last five years in the Institute of A...
Conjugated cyclic trienes without nonbenzenoid aromatic characteristic were successfully employed as...
The thermal 1,3-dipolar cycloaddition of unactivated azomethine ylides derived from allylamine and a...
Catalytic enantioselective tandem carbonyl ylide formation-cycloaddition reactions of tert-butyl 2-d...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...