Abstract
New 2′-iodo-N-phenyl-1-tosyl-spiro[3,1-benzoxazine-4,1′-cycloalkan]-2-imines have been synthesized by reacting N-tosyl-N-(2-cycloalk-1-en-1-ylphenyl)-N′-phenylureas with iodine at room temperature.
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ACKNOWLEDGMENTS
The spectral analyses were carried out using the facilities of joint center at the Ufa Institute of Chemistry (Russian Academy of Sciences).
Funding
This study was performed in the framework of the program “New Approaches and Improvement of Known Strategies for Target-Oriented Synthesis of Poly-, Bi-, and Monocyclic N,N-, N,O-, and S,O-Heterocycles, Study of Their Biological and Anticorrosion Activities, and Development of Technologies for Practical Application of the Obtained Compounds with Appropriate Properties” (state registration no. 122031400274-4).
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Translated from Zhurnal Organicheskoi Khimii, 2022, Vol. 58, No. 10, pp. 1063–1070 https://doi.org/10.31857/S0514749222100032.
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Musabirov, I.Z., Gataullin, R.R. Synthesis of 1-Tosylspiro[3,1-benzoxazine-4,1′-cycloalkan]-2-imines. Russ J Org Chem 58, 1403–1408 (2022). https://doi.org/10.1134/S1070428022100037
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DOI: https://doi.org/10.1134/S1070428022100037