Highly stereoselective synthesis of spirocyclopropylthiooxindoles and biological evaluation

Stereochemically rich spirocycles are greatly sought-after structures for drug discovery. The development of efficient and flexible methods capable of constructing spirocycles derived from privileged scaffolds with structural diversity in a highly diastereo- and enantioselective manner is of current interest. Here, we present a novel highly stereoselective Rh-catalyzed olefin cyclopropanation of diazothiooxindoles for the facile access of optically active spirocyclopropylthiooxindoles in high to excellent enantiomeric excess. Notably, our protocol is compatible with a broad range of a-functionalized styrenes, allowing the merger of other pharmacophores such as fluoroalkyl, boron moiety, and silyl groups with spirocyclic thiooxindoles. Moreover, antiproliferative activity assessment shows that compounds 3e, 4a, and 4j displayed the most potent antiproliferation effect against MCF-7, HCT116, and SJSA-1 cells (IC50 = 1.09, 2.05, and 0.82 mu M, respectively) without affecting normal cells.

Automated summary

This study presents a highly stereoselective catalytic reaction for the construction of spirocycles. The synthesized compounds exhibit potent antiproliferative activity and have the potential for the treatment of various diseases.