Abstract
The catalytic dehydrocyclization of 3-isopropyl-2,6-diphenylpyridine proceeds in two directions: conversion to 10-methyl-3-phenyl-4-azaphenanthrene and conversion to 9,9-dimethyl-4-azafluorene. C(9)-Unsubstituted 4-azafluorenes were obtained in the dehydrocyclization of pyridine bases that contain a phenyl group in the α position and an n-propyl group in the β position.
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 648–650, May, 1984.
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Prostakov, N.S., Varlamov, A.V. & Borisova, T.N. Catalytic dehydrocyclization of 3-isopropyl(n-propyl)-2,6-diphenylpyridine and 3-n-propyl-2,4,6-triphenylpyridine. Chem Heterocycl Compd 20, 519–521 (1984). https://doi.org/10.1007/BF00514305
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DOI: https://doi.org/10.1007/BF00514305