The spirooxindole system is the core structure of a variety of medicinal agents and natural
products. 1, 2 In fact, spirooxindole derivatives have been described with different biological …

This review provides the authors' selection of recent publications that highlight the
increasing efforts to develop valuable organocatalytic domino/tandem/cascade reactions as …

An unprecedented organocatalytic asymmetric Michael/cyclization cascade reaction of 3-
isothiocyanato oxindoles and 3-nitroindoles has been disclosed. A wide range of …

Abstract α‐Isothiocyanato amides, esters and phosphonates have emerged as new types of
versatile reagents for various organo‐and metal‐catalyzed asymmetric cascade reactions …

An efficient organocatalytic diastereo-and enantioselective method for the construction of
spirocyclic oxindole derivatives bearing two spiro quaternary centers and three consecutive …

An asymmetric cascade Mannich/cyclization reaction between 3-isothiocyanato oxindoles
and sulfimides using a commercially available organocatalyst has been developed. A wide …

An efficient, clean, atom-economical and simple method for the one-pot synthesis of novel
spirooxindole derivatives via a three-component reaction of isatins, dimedone and …

An efficient method for the direct construction of two classes of spirocyclic oxindoles by the
reactions of 3-hydroxyoxindoles/3-aminooxindoles and (Z)-olefinic azlactones through a …

Abstract An efficient asymmetric [3+ 2]-cycloaddition reaction of 3-isothiocyanato oxindoles
and formaldimines in-situ generated from 1, 3, 5-trisubstituted-hexahydro-1, 3, 5-triazines …

Spirooxindole moiety is an important heterocyclic framework that is present as the core
structural unit in several biologically active synthetic and naturally occurring molecules. The …