Abstract
Cationic cyclizations of N-phenacyl-4-aryl-1,2,3,6-tetrahydropyridines and related compounds were studied, and structures I products formed were elucidated using NMR spectroscopy.
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Additional information
Institute for Drug Research, Ltd. H-1045 Budapest, Berlini-u 47-49, Hungary. Published in Khimiya Geterotsiklicheskikh Soedinenii, No. 10, pp. 1367–1372, October, 1995. Original article submitted August 24, 1995.
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Sólyom, S., Csuzdi, E. & Ábrahám, G. Expected and unexpected intramolecular cationic cyclizations. Chem Heterocycl Compd 31, 1196–1200 (1995). https://doi.org/10.1007/BF01185589
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DOI: https://doi.org/10.1007/BF01185589