The asymmetric organocatalysis is definitely one of the most powerful and versatile tools for the rapid construction of various spirocyclic oxindoles. In the past few years, a number of successful strategies based on organocatalysis have been developed for the construction of 3,3-spirocyclic oxindoles in high yields and excellent enantioselectivities under mild conditions. In this review, recent advances in this area are summarized and classified according to the spiro ring fused at the 3-position of the oxindole core.Department of Applied Biology and Chemical Technolog
In recent years, organocatalysis has enhanced its importance as a tool for the synthesis of enantiom...
The first enantioselective organocatalytic two- and three-component reactions via a domino Knoevenag...
Following the reactivity inversion strategy, two different two-step sequences were designed and succ...
The spiro[pyrrodilin-3,3’-oxindole] ring skeleton is a privileged structure with promising biologic...
Oxindoles containing a spiro quaternary stereogenic center as part of a pyrrolidinyl or cyclohexyl r...
A new and flexible methodology catalyzed by bifunctional chiral thioureas has been developed to reac...
3-Chlorooxoindoles have emerged as versatile precursors in the synthesis of spirocyclopropyl oxindol...
An unprecedented organocatalytic asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato...
The asymmetric synthesis of 3‐substituted oxindoles is a topic of considerable importance because th...
Indole derivatives are the most common heterocycle compounds present in nature, for this reason, the...
The thesis entitled “Organocatalytic Cascade Cyclizations for the Enantioselective Synthesis of Spir...
An unprecedented organocatalytic asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato...
In recent years, organocatalysis has enhanced its importance as a tool for the synthesis of enantiom...
In recent years, organocatalysis has enhanced its importance as a tool for the synthesis of enantiom...
A novel organocatalytic strategy for the synthesis of highly substituted spirocyclopentaneoxindoles ...
In recent years, organocatalysis has enhanced its importance as a tool for the synthesis of enantiom...
The first enantioselective organocatalytic two- and three-component reactions via a domino Knoevenag...
Following the reactivity inversion strategy, two different two-step sequences were designed and succ...
The spiro[pyrrodilin-3,3’-oxindole] ring skeleton is a privileged structure with promising biologic...
Oxindoles containing a spiro quaternary stereogenic center as part of a pyrrolidinyl or cyclohexyl r...
A new and flexible methodology catalyzed by bifunctional chiral thioureas has been developed to reac...
3-Chlorooxoindoles have emerged as versatile precursors in the synthesis of spirocyclopropyl oxindol...
An unprecedented organocatalytic asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato...
The asymmetric synthesis of 3‐substituted oxindoles is a topic of considerable importance because th...
Indole derivatives are the most common heterocycle compounds present in nature, for this reason, the...
The thesis entitled “Organocatalytic Cascade Cyclizations for the Enantioselective Synthesis of Spir...
An unprecedented organocatalytic asymmetric Michael/cyclization cascade reaction of 3-isothiocyanato...
In recent years, organocatalysis has enhanced its importance as a tool for the synthesis of enantiom...
In recent years, organocatalysis has enhanced its importance as a tool for the synthesis of enantiom...
A novel organocatalytic strategy for the synthesis of highly substituted spirocyclopentaneoxindoles ...
In recent years, organocatalysis has enhanced its importance as a tool for the synthesis of enantiom...
The first enantioselective organocatalytic two- and three-component reactions via a domino Knoevenag...
Following the reactivity inversion strategy, two different two-step sequences were designed and succ...