A general strategy for the construction of X-azabicyclo[m.2.1]alkane frameworks in optically pure form is reported by the asymmetric [3+2]-cycloaddition reaction of cyclic azomethine ylides with Oppolzer's acryloyl camphor sultam
We provide a comprehensive account of the 1,3-dipolar cycloaddition reactions of azomethine ylides w...
A new formal [3 + 1]-cycloaddition reaction of azaoxyallyl cation intermediates, generated in situ f...
A novel organocatalytic formal [3 + 2] cycloaddition reaction with in situ generation of N-carbamoyl...
Various new structural entities related to x-azatricyclo[m.n.0.0a,b]alkanes are constructed by the i...
A new and general strategy for the stereoselective construction of X-azabicyclo[m.2.1]alkanes has be...
The intermolecular 1,3-dipolar cycloaddition reaction of azomethine ylides with carbon-carbon double...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddit...
CONSPECTUS: Cycloaddition reactions are among the most powerful methods for the synthesis of complex...
International audienceThe use of structurally similar chiral non-racemic azomethine ylides, nitrones...
Our interest in the synthesis of compact nitrogen heterocycles from abundant sources has motivated a...
The completion of the total synthesis of Kopsia lapidilecta alkaloid (+/-)-lapidilectine B is descri...
This review highlights the biological importance of many polysubstituted nitro-prolines and -pyrroli...
Summary: Development of a general catalytic and highly efficient method utilizing readily available ...
N-Metallated azomethine ylides 5 were generated by the reaction of arylidene glycine imines 1 with A...
We provide a comprehensive account of the 1,3-dipolar cycloaddition reactions of azomethine ylides w...
A new formal [3 + 1]-cycloaddition reaction of azaoxyallyl cation intermediates, generated in situ f...
A novel organocatalytic formal [3 + 2] cycloaddition reaction with in situ generation of N-carbamoyl...
Various new structural entities related to x-azatricyclo[m.n.0.0a,b]alkanes are constructed by the i...
A new and general strategy for the stereoselective construction of X-azabicyclo[m.2.1]alkanes has be...
The intermolecular 1,3-dipolar cycloaddition reaction of azomethine ylides with carbon-carbon double...
International audienceTwo types of bicyclic N-cyclopropyl glycine ester derivatives have been prepar...
Two complementary approaches to substituted pyrrolidines via stereocontrolled 1,3-dipolar cycloaddit...
CONSPECTUS: Cycloaddition reactions are among the most powerful methods for the synthesis of complex...
International audienceThe use of structurally similar chiral non-racemic azomethine ylides, nitrones...
Our interest in the synthesis of compact nitrogen heterocycles from abundant sources has motivated a...
The completion of the total synthesis of Kopsia lapidilecta alkaloid (+/-)-lapidilectine B is descri...
This review highlights the biological importance of many polysubstituted nitro-prolines and -pyrroli...
Summary: Development of a general catalytic and highly efficient method utilizing readily available ...
N-Metallated azomethine ylides 5 were generated by the reaction of arylidene glycine imines 1 with A...
We provide a comprehensive account of the 1,3-dipolar cycloaddition reactions of azomethine ylides w...
A new formal [3 + 1]-cycloaddition reaction of azaoxyallyl cation intermediates, generated in situ f...
A novel organocatalytic formal [3 + 2] cycloaddition reaction with in situ generation of N-carbamoyl...