Abstract
The acid-catalyzed rearrangement of 2,5-dimethoxytetrahydrofuryl-3-carbinol, obtained from 2,5-dimethoxy-3-formyltetrahydrofuran, gave the 2-substituted 3-formyl-5-methoxytetrahydrofuran.
This is a preview of subscription content, log in via an institution to check access.
Similar content being viewed by others
Literature Cited
D. Degner, A. Friedenrang, H. Siegel, and T. Simenc, Chem. Abstr., 89, 112227 (1978).
T. Shono, Y. Matsumura, and H. Hamaguchi, J. Chem. Soc., Chem. Commun., No. 20, 712 (1977).
N. Clauson-Kaas, P. Dietrich, and J. Nielsen, Acta Chem. Scand., 7, 845 (1953).
Author information
Authors and Affiliations
Additional information
Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 2, pp. 164–166, February, 1991.
Rights and permissions
About this article
Cite this article
Brezhnev, L.Y., Vartanyan, M.M. & Khandin, A.V. Synthesis of 2-substituted 3-formyl-5-methoxy-tetrahydrofurans from 2,5-dimethoxytetrahydrofuryl-3-carbinols. Chem Heterocycl Compd 27, 132–134 (1991). https://doi.org/10.1007/BF00476742
Received:
Issue Date:
DOI: https://doi.org/10.1007/BF00476742