An efficient one pot asymmetric synthesis of tetrahydropyrano[2,3-<i>c</i>]pyrazoles has been developed. This class of biologically active heterocycles can be obtained via a secondary amine catalyzed asymmetric Michael/Wittig/oxa-Michael reaction sequence. Remarkably, the title compounds were accessible in good to very good yields and very good to excellent enantioselectivities after a single purification step
A new bifunctional squaramide organocatalyst derived from l-proline mediated the first enantioselect...
An efficient enantioselective formal [3 + 2]-cycloaddition of azomethine imines with azlactones has ...
The first organocatalytic diastereo- and enantioselective Michael addition reaction of 4-substituted...
This thesis explores the applications of organocatalysis and its combination with metal catalysis fo...
An efficient one‐pot asymmetric synthesis of pyrazoles bearing a chiral quaternary stereocenter has ...
A diastereo- and enantioselective Michael/Henry/ketalization sequence to functionalized tetrahydropy...
The first diastereo- and enantioselective synthesis of spiro-tetrahydrofuran-pyrazolones is reported...
Diastereoisomeric pyrazolone-fused spirocyclohexenimines, bearing contiguous all-carbon quaternary a...
The first organocatalytic double Michael cascade reaction between unsaturated ketones and unsaturate...
Recent advancement in the area of asymmetric organocatalysis led to the development of new methodolo...
1,2,3,4-Tetrahydropyrrolo[1,2-a]pyrazines are an important motif due to their biological activities ...
An organocatalytic asymmetric cascade Michael/hemiketalization/retro-aldol reaction between unsatura...
The asymmetric total synthesis of pyranicin (1) is reported. The butenolide ring was constructed via...
A quinine‐derived thiourea catalysed the enantioselective addition of 4‐substituted pyrazolones to i...
1,2,3,4-Tetrahydropyrrolo1,2-apyrazines are an important motif due to their biological activities an...
A new bifunctional squaramide organocatalyst derived from l-proline mediated the first enantioselect...
An efficient enantioselective formal [3 + 2]-cycloaddition of azomethine imines with azlactones has ...
The first organocatalytic diastereo- and enantioselective Michael addition reaction of 4-substituted...
This thesis explores the applications of organocatalysis and its combination with metal catalysis fo...
An efficient one‐pot asymmetric synthesis of pyrazoles bearing a chiral quaternary stereocenter has ...
A diastereo- and enantioselective Michael/Henry/ketalization sequence to functionalized tetrahydropy...
The first diastereo- and enantioselective synthesis of spiro-tetrahydrofuran-pyrazolones is reported...
Diastereoisomeric pyrazolone-fused spirocyclohexenimines, bearing contiguous all-carbon quaternary a...
The first organocatalytic double Michael cascade reaction between unsaturated ketones and unsaturate...
Recent advancement in the area of asymmetric organocatalysis led to the development of new methodolo...
1,2,3,4-Tetrahydropyrrolo[1,2-a]pyrazines are an important motif due to their biological activities ...
An organocatalytic asymmetric cascade Michael/hemiketalization/retro-aldol reaction between unsatura...
The asymmetric total synthesis of pyranicin (1) is reported. The butenolide ring was constructed via...
A quinine‐derived thiourea catalysed the enantioselective addition of 4‐substituted pyrazolones to i...
1,2,3,4-Tetrahydropyrrolo1,2-apyrazines are an important motif due to their biological activities an...
A new bifunctional squaramide organocatalyst derived from l-proline mediated the first enantioselect...
An efficient enantioselective formal [3 + 2]-cycloaddition of azomethine imines with azlactones has ...
The first organocatalytic diastereo- and enantioselective Michael addition reaction of 4-substituted...