1. INTRODUCTION Indoline-2, 3-dione or indole-1H-2, 3-dione (Figure 1), commonly known
as isatin, is a well-known natural product found in plants of genus Isatis and in Couropita …

The review highlights the hydantoin syntheses presented from the point of view of the
preparation methods. Novel synthetic routes to various hydantoin structures, the advances …

The structural elucidation of chiral rare-earth-based catalysts in asymmetric reactions holds
significant importance as it is crucial for comprehending their operational mechanisms and …

The organocatalytic enantioselective decarboxylative addition of malonic acid half thioesters
to ketimines derived from isatins by using N‐heteroarenesulfonyl cinchona alkaloid amides …

3-Amino-2-oxindoles bearing tetra-substituted stereocenter are very important constituents
of many bioactive and pharmaceutical agents. In the last few years, asymmetric …

3-Substituted-3-aminooxindoles have attracted the attention of organic and medicinal
chemists because these motifs constitute the core structure of a number of natural products …

We report the first catalytic asymmetric cyanation of N-Boc ketoimines, which enables highly
enantioselective synthesis of oxindole based α-amino nitriles. An unprecedented tandem …

Get selective! Enantioselective allylation of ketimines derived from isatins by using chiral 1, 3‐
bis (imidazolin‐2‐yl) benzene (Phebim)–PdII complexes afforded products with good …

A catalytic enantioselective Strecker reaction of isatin-derived N-unsubstituted ketimines
directly afforded the N-unprotected α-aminonitriles with a tetrasubstituted carbon …

An organocatalytic enantioselective Strecker reaction for the synthesis of 3‐amino‐3‐
cyanooxindoles has been developed. Employing a quinine‐derived thiourea catalyst, the …