Issue 76, 2024

Pd-catalyzed sequential intramolecular annulation/intermolecular [3+2] cycloaddition of 5-allenyloxazolidine-2,4-diones with dipoles: synthesis of spiroheterocycles

Abstract

Pd-catalyzed sequential intramolecular annulation/intermolecular [3+2] cycloaddition of 5-allenyloxazolidine-2,4-diones with dipoles was achieved. Under palladium catalysis, various 5-allenyloxazolidine-2,4-diones reacted with 1,3-dipoles such as nitrile N-oxides, azomethine imines or nitrilimines to give a series of functionalized spiroheterocycles in high yields. The scale-up reaction and further derivation of products were successful. A plausible mechanism was also proposed based on the control experiments.

Graphical abstract: Pd-catalyzed sequential intramolecular annulation/intermolecular [3+2] cycloaddition of 5-allenyloxazolidine-2,4-diones with dipoles: synthesis of spiroheterocycles

Supplementary files

Article information

Article type
Communication
Submitted
16 Jul 2024
Accepted
24 Aug 2024
First published
26 Aug 2024

Chem. Commun., 2024,60, 10516-10519

Pd-catalyzed sequential intramolecular annulation/intermolecular [3+2] cycloaddition of 5-allenyloxazolidine-2,4-diones with dipoles: synthesis of spiroheterocycles

Y. Dong, J. Liu, R. Ning, F. Yang, C. Zhang and H. Guo, Chem. Commun., 2024, 60, 10516 DOI: 10.1039/D4CC03551H

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