Abstract
PMR spectroscopy was used to show that the hydrazones of (2-benzothiazolyl) and (2-benzoxazolyl)acetic acids exist in solution as equilibrium mixtures of stereoisomeric forms due to conformational and geometric isomerism.
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References
I. P. Bezhan, V. A. Khrustalev, K. N. Zelenin, and B. P. Nikolaev, Zh. Org. Khim.,14, 754 (1978).
K. N. Zelenin, V. V. Pinson, A. A. Potekhin, I. P. Bezhan, V. A. Khrustalev,and P. S. Lobanov, Zh. Org. Khim.,14, 490 (1978).
S. I. Yakimovich, V. N. Nikolaev, and O. A. Afonina, Zh. Org. Khim.,15, 922 (1979).
A. I. Rutavichyus and S. P. S. P. Valyulene, Trudy Akad. Nauk Lithuanian SSR, Ser. B, 4(155), 61 (1986).
V. G. Yusupov, S. I. Yakimovich, S. D. Nasirdinov, and S. D. Parpiev, Zh. Org. Khim.,16, 415 (1980).
Additional information
Institute of Chemistry, 2600 Vilnius, Lithuania. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 708-712, May, 1995. Original article submitted April 3, 1995.
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Rutavlcius, A., Valiulene, S. & Kuodis, Z. Isomerism of hydrazones of (2-benzothiazolylthio)- and (2-benzoxazolylthio)acetic acids. Chem Heterocycl Compd 31, 629–633 (1995). https://doi.org/10.1007/BF01166343
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DOI: https://doi.org/10.1007/BF01166343