“…The reaction was rapid, high yielding, and a non-chromatographic purication protocol was used. 184 In 2021, Maniam et al designed a green and rapid methodology for the synthesis of spirooxindole pyrrolizidines (39) employing a microwave-assisted one-pot, three-component 1,3dipolar cycloaddition of azomethine ylides from L-proline (11) and isatin (1) with various b-nitrostyrenes (38) in methanol as the solvent at 65 °C to obtain products in reasonable-to-high yields (Scheme 13). 185 The structure of (1 0 R,2 0 R,3R)-2 0 -(2,4-dimethoxyphenyl)-1 0nitro-1 0 ,2 0 ,5 0 ,6 0 ,7 0 ,7a 0 -hexahydrospiro[indoline-3,3 0 -pyrrolizin]-2- one (39) was conrmed by single-crystal X-ray analysis.…”