Issue 24, 1995

Trifluoromethanesulfonic anhydride–4-(N,N-dimethylamino)pyridine as a reagent combination for effecting Bischler–Napieraiski cyclisation under mild conditions: application to total syntheses of the Amaryllidaceae alkaloids N-methylcrinasiadine, anhydrolycorinone, hippadine and oxoassoanine

Abstract

A combination of triflic anhydride and 4-(N,N-dimethylamnino)pyridine effects Bischler–Napieraiski cyclisation of β-phenethytearbamates and β-phenethylamides under very mild conditions.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1995, 2551-2553

Trifluoromethanesulfonic anhydride–4-(N,N-dimethylamino)pyridine as a reagent combination for effecting Bischler–Napieraiski cyclisation under mild conditions: application to total syntheses of the Amaryllidaceae alkaloids N-methylcrinasiadine, anhydrolycorinone, hippadine and oxoassoanine

M. G. Banwell, B. D. Bissett, S. Busato, C. J. Cowden, D. C. R. Hockless, J. W. Holman, R. W. Read and A. W. Wu, J. Chem. Soc., Chem. Commun., 1995, 2551 DOI: 10.1039/C39950002551

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