Access to highly enantioselective and diastereoselective spirooxindole dihydrofuran fused pyrazolones†
Prakash K. Warghude,Abhijeet S. Sabale,Ramakrishna G. Bhat
Organic & Biomolecular Chemistry Pub Date : 02/11/2020 00:00:00 , DOI:10.1039/D0OB00007H
Abstract

A tertiary amine catalyzed highly diastereoselective and enantioselective [3 + 2] annulation between Morita–Baylis–Hillman (MBH) carbonates derived from isatin and pyrazolone 4,5-diones has been developed. A series of structurally diverse and multifunctional spirooxindole dihydrofuran fused pyrazolone derivatives with two adjacent quaternary spirocenters has been achieved in excellent yields with good to excellent enantioselectivity. Further synthetic utility of this protocol has been successfully demonstrated by employing the bromo derivative of spirooxindole dihydrofuran fused pyrazolone to Suzuki coupling.

Graphical abstract: Access to highly enantioselective and diastereoselective spirooxindole dihydrofuran fused pyrazolones