Abstract
Tetrahydrofuro[2,3-b]indole derivatives are formed by refluxing arylhydrazine salts in alcohol with γ-hydroxy ketones that have an α-methylidyne group.
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I. I. Grandberg and S. N. Dashkevich, Izv. Se'lskokhoz. Akad. im. Timiryazeva, 1, 189 (1971).
I. I. Grandberg and S. N. Dashkevich, Khim. Geterotsikl. Soedin., 1631 (1970).
I. I. Grandberg and S. N. Dashkevich, Khim. Geterotsikl. Soedin., 342 (1971).
R. B. Longmore and B. Robinson, Coll., 32, 2148 (1967).
J. Brand and G. Eglinton, Application of Spectroscopy in Organic Chemistry [Russian translation], Mir, Moscow (1967), p. 128.
N. V. Kuznetsov and R. A. Myrsina, Ukr. Khim. Zh., 35, 530 (1969).
I. S. Trubnikov and Yu. A. Pentin, Zh. Obshch. Khim., 32, 3590 (1962).
I. I. Grandberg and T. P. Moskvina, Khim. Geterotsikl. Soedin., 942 (1970).
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See [1] for communication XXII.
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 782–786, June, 1971.
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Grandberg, I.I., Dashkevich, S.N. Indoles. Chem Heterocycl Compd 7, 729–733 (1971). https://doi.org/10.1007/BF00476820
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DOI: https://doi.org/10.1007/BF00476820