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Preparation of stereoisomeric amino alcohols of the furan series

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Chemistry of Heterocyclic Compounds Aims and scope

Abstract

The reaction of stereoisomers of 2, 5-dialkoxy-3, 4-epoxytetrahydrofuran with secondary amines has given stereoisomers of 2, 5-dialkoxy-4-dialkylamino-3-hydroxytetrahydrofuran. Their configuration have been confirmed by IR spectroscopy.

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References

  1. L. N. Kralinina, R. I. Kruglikova, V. V. Yastrebov, G. P. Krutetskaya, G. I. Samokhvalov, and A. I. Chernyshev, KhGS [Chemistry of Heterocyclie Compounds], collection 2, 1970 (in the press).

  2. E. Eliel, W. Allinger, S. Angyal, and J. Morrison, Conformational Analysis, New York, 200, 1965.

  3. A. Stoll, E. Gucker, and R. Suess, German patent no. 951570, 1956; C. A., 53, 16150, 1959.

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Authors and Affiliations

  1. Lomonosov Moscow Institute of Fine Chemical Technology, USSR

    L. N. Kralinina, R. I. Kruglikova & V. I. Bogomolova

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  1. L. N. Kralinina
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  2. R. I. Kruglikova
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  3. V. I. Bogomolova
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Kralinina, L.N., Kruglikova, R.I. & Bogomolova, V.I. Preparation of stereoisomeric amino alcohols of the furan series. Chem Heterocycl Compd 6, 280–281 (1970). https://doi.org/10.1007/BF00471219

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  • DOI: https://doi.org/10.1007/BF00471219

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