Cross-conjugated trienamines are introduced as a new concept in asymmetric organocatalysis. These intermediates are applied in highly enantioselective Diels–Alder and addition reactions, providing functionalized bicyclo[2.2.2]octane compounds and γ′-addition products, respectively. The nature of the transformations and the intermediates involved are investigated by computational calculations and NMR analysis
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
We report a synthetic strategy for a chemoselective switch and a diastereo-divergent approach for th...
The first examples of [3+2] cycloaddition reactions between 3,3,3-tribromo-1-nitroprop-1-ene (TBMN) ...
Cross-conjugated trienamines are introduced as a new concept in asymmetric organocatalysis. These in...
ABSTRACT: Cross-conjugated trienamines are intro-duced as a new concept in asymmetric organocatalysi...
The Diels–Alder reactions of cyclic linear and cross-conjugated trienamines with oxindoles have been...
The 1,4-conjugate addition of nucleophiles to \u3b1,\u3b2-unsaturated carbonyl compounds represents ...
A new concept in organocatalysis allowing for the construction of cyclobutanes with four contiguous ...
A diastereodivergent approach to highly substituted bicyclo[3.1.0]hexanes has been developed throug...
After prosperous domino reactions towards benzopyrans, the products were used as the starting materi...
A novel organocatalytic formal [3 + 2] cycloaddition reaction with in situ generation of N-carbamoyl...
In this manuscript, we are particularly interested in the formation of chiral mono- and polycyclic c...
Modulation of the complex reactivity of cyclohexenylidene malononitriles using diverse \u3b2-aryl-su...
Modulation of the complex reactivity of cyclohexenylidene malononitriles using diverse β-aryl-substi...
In this article we describe a series of new asymmetric Michael reactions of carboxylate-3-substitute...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
We report a synthetic strategy for a chemoselective switch and a diastereo-divergent approach for th...
The first examples of [3+2] cycloaddition reactions between 3,3,3-tribromo-1-nitroprop-1-ene (TBMN) ...
Cross-conjugated trienamines are introduced as a new concept in asymmetric organocatalysis. These in...
ABSTRACT: Cross-conjugated trienamines are intro-duced as a new concept in asymmetric organocatalysi...
The Diels–Alder reactions of cyclic linear and cross-conjugated trienamines with oxindoles have been...
The 1,4-conjugate addition of nucleophiles to \u3b1,\u3b2-unsaturated carbonyl compounds represents ...
A new concept in organocatalysis allowing for the construction of cyclobutanes with four contiguous ...
A diastereodivergent approach to highly substituted bicyclo[3.1.0]hexanes has been developed throug...
After prosperous domino reactions towards benzopyrans, the products were used as the starting materi...
A novel organocatalytic formal [3 + 2] cycloaddition reaction with in situ generation of N-carbamoyl...
In this manuscript, we are particularly interested in the formation of chiral mono- and polycyclic c...
Modulation of the complex reactivity of cyclohexenylidene malononitriles using diverse \u3b2-aryl-su...
Modulation of the complex reactivity of cyclohexenylidene malononitriles using diverse β-aryl-substi...
In this article we describe a series of new asymmetric Michael reactions of carboxylate-3-substitute...
Nowadays, organocatalysis constitutes the third pillar of asymmetric catalysis, alongside transition...
We report a synthetic strategy for a chemoselective switch and a diastereo-divergent approach for th...
The first examples of [3+2] cycloaddition reactions between 3,3,3-tribromo-1-nitroprop-1-ene (TBMN) ...