Issue 16, 1984

Trapping of cyclopentadienone as a 4π component in Diels–Alder reactions with ethyl acrylate: a simple synthesis of (±)-sarkomycin

Abstract

The ability of cyclopentadienone to act as the diene counterpart in Diels–Alder reactions was demonstrated through the isolation of the cycloadduct with ethyl acrylate, which was utilized as the starting point for an expeditious synthesis of (±)-sarkomycin.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1984, 1049-1050

Trapping of cyclopentadienone as a 4π component in Diels–Alder reactions with ethyl acrylate: a simple synthesis of (±)-sarkomycin

P. G. Baraldi, A. Barco, S. Benetti, G. P. Pollini, E. Polo and D. Simoni, J. Chem. Soc., Chem. Commun., 1984, 1049 DOI: 10.1039/C39840001049

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