Publications by authors named "S S Chimni"

The organocatalytic asymmetric synthesis of enantiopure bis-heterocyclic molecules containing pyrazole and isoxazole under mild reaction conditions has been reported a low-catalyst loading Michael addition reaction of pyrazolyl nitroalkenes with 1,3-dicarbonyl derivatives. 4-Substituted pyrazole derivatives were obtained in 60-87% yields and with 82-97% ee. These pyrazolyl derivatives are further transformed into chiral bis-heterocyclic derivatives in up to 82% yields and up to 99% ee.

View Article and Find Full Text PDF

Phenolics are the most abundant secondary metabolites of plants that are widely distributed in the plant kingdom. In the last few years, the development and identification of phenolic compounds from various plants have become a major area of the environment and health-related research. In the present study, different phenolic compounds were purified from the bark of the medicinally important plant Acacia nilotica which is rich in polyphenols and were evaluated for their insecticidal potential against a polyphagous pest, Spodoptera litura (Fab.

View Article and Find Full Text PDF

Arenesulfonyl indoles, bearing a good leaving group, are effective precursors for vinylogous imine intermediates which are generated under basic conditions. This intermediate can readily react with other nucleophilic reagents to obtain C-3 substituted indole derivatives. In the last few years, a plethora of exciting synthetic applications of this substrate have been exploited.

View Article and Find Full Text PDF
Article Synopsis
  • Candida antarctica (CAL-B) lipase was used to effectively resolve 1,3-dialkyl-3-hydroxymethyl oxindoles, yielding (R)- and (S)- forms with high optical purity (99% ee and 78% ee, respectively).
  • Vinyl acetate was used as the acylating agent alongside acetonitrile as a solvent in the reaction process.
  • The resulting optically active compounds, including 3-substituted-3-hydroxymethyl oxindoles and spiro-oxindoles, are important precursors for synthesizing potentially biologically active molecules.
View Article and Find Full Text PDF

3-Substituted-3-aminooxindoles are versatile scaffolds and they are common core structural motifs found in many natural products and biologically active compounds. In the last few years, a variety of synthetic methodologies have been developed for the synthesis of this moiety. In this review, we are presenting the recent advances in the catalytic synthesis of 3-aminooxindole derivatives.

View Article and Find Full Text PDF