Cycloaddition of nitrilimine to R–(−)-Carvone

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Abstract

Cycloaddition of nitrilimine generated in situ from N-phenylbenzene carbohydrazonoyl chloride in the presence of triethylamine affords (3aS,5R,7aS)-5-isopropenyl-7a-methyl-1,3-diphenyl-1,3a,4,5,6,7a-hexahydro-7H-indazol-7-one as the main reaction product. The structure of the resulting compound was determined by spectral methods.

About the authors

N. R Yamaletdinova

Ufa Institute of Chemistry, Ufa Federal Research Center, Russian Academy of Sciences

Email: gataullin@anrb.ru
Ufa, Russia

R. R Safargalin

Ufa Institute of Chemistry, Ufa Federal Research Center, Russian Academy of Sciences

Email: gataullin@anrb.ru
ORCID iD: 0009-0007-9462-9027
Ufa, Russia

R. R Gataullin

Ufa Institute of Chemistry, Ufa Federal Research Center, Russian Academy of Sciences

Author for correspondence.
Email: gataullin@anrb.ru
ORCID iD: 0000-0003-3269-2729
Ufa, Russia

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