Issue 23, 1972

Nuclear synthesis of 1,4-dihydropyridines by rearrangement of aziridinobicyclo[2,2,1]pyridazine carboxylates

Abstract

The adducts of cyclopentadiene and azodicarboxylate esters were treated with benzenesulphonyl azide producing the fused aziridine derivatives, (4) and (5); hydrolysis of the ethyl ester (4) gave the diazatricylene (7) whereas hydrolysis of the t-butyl ester led to the dihydropyridine (9).

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1972, 1260-1261

Nuclear synthesis of 1,4-dihydropyridines by rearrangement of aziridinobicyclo[2,2,1]pyridazine carboxylates

A. I. Meyers, D. M. Stout and T. Takaya, J. Chem. Soc., Chem. Commun., 1972, 1260 DOI: 10.1039/C39720001260

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