How to cite this paper
Kachaeva, M., Pilyo, S., Popilnichenko, S., Kornienko, A., Rusanov, E., Prokopenko, V., Zyabrev, V & Brovarets, V. (2018). Synthesis of fused heterocycles from 2-aryl-5-(chlorosulfonyl)-1,3-oxazole-4-carboxylates and α-aminoazoles involving the Smiles rearrangement.Current Chemistry Letters, 7(4), 101-110.
Refrences
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5. Pozharskii A. F., Soldatenkov A. T., and Katritzky A. R. (2011) Heterocycles in Life and Society, 2th Ed, Wiley, 144–146.
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7. Ege G., and Franz H. (1984) Aminopyrazoles. V [1]. Structure assignment of lH-pyrazol-3- and 5 amines by means of the 1H NMR δ(4-H)-values of their exo-N-toluenesulfonyl derivatives. J. Heterocyclic Chem., 21 (3) 689–695.
8. Backer H. J., and De Jonge J. (1943) Dérivés de la sulfanilamide renfermant l'anneau 1,2,4‐triazol. Recl. Trav. Chim. Pays-Bas., 62 (3) 158–162.
9. Plesniak K., Zarecki A., and Wicha J. (2007) The smiles rearrangement and the Julia-Kocienski olefination reaction. Top. Curr. Chem., 275 (46) 163–250.
10. Plescia S., Agozzino P, and Fabra I. (1977) A facile synthesis of some pyrazolo[1,5-b]-1,2,4-benzothiadiazepin-5(4H)ones-10,10-dioxides. A new ring system. J. Heterocyclic Chem., 14 (8) 1431–1432.
11. Sheldrick G. (2008) A short history of SHELX. Acta Cryst., Sect. A., 64 (Pt 1) 112–122.
2. Barbey S., Goossens L., Taverne T., Cornet J., Choesmel V., Rouaud C., Gimeno G., Yannic-Arnoult S., Michaux C., Charlier C., Houssin R., and Henichart J.-P. (2002) Synthesis and activity of a new methoxytetrahydropyran derivative as dual cyclooxygenase-2/5-lipoxygenase inhibitor. Bioorg. Med. Chem. Lett., 12 (5) 779–782.
3. Kachaeva M. V., Pilyo S. G., Kornienko A. M., Prokopenko V. M., Zhirnov V. V., Prichard M. N., Keith K. A., Yang G., Wang H.-K., Banerjee N. S., Chow L. T., Broker T. R., and Brovarets V. S. (2017) In vitro activity of novel 1,3-oxazole derivatives against human papillomavirus. Ibnosina J. Med. Biomed. Sci., 9 (4) 111–118.
4. Kornienko A. N., Pil'o S. G., Prokopenko V. M., and Brovarets V. S. (2014) Synthesis of methyl 2-aryl-5-chlorosulfonyl-1,3-oxazole-4-carboxylates and their reactions with amines and amidines Rus. J. Gen. Chem., 84 (8) 1555–1560.
5. Pozharskii A. F., Soldatenkov A. T., and Katritzky A. R. (2011) Heterocycles in Life and Society, 2th Ed, Wiley, 144–146.
6. Kornienko A. N., Pil’o S. G., Kozachenko A. P., Prokopenko V. M., Rusanov E. B., and Brovarets V. S. (2014) Reaction of 2-aryl-4-cyano-1,3-oxazole-5-sulfonyl chlorides with 5-amino-1H-pyrazoles and 5-amino-1H-1,2,4-triazole. Chem. Het. Comp., 50 (1) 76–86.
7. Ege G., and Franz H. (1984) Aminopyrazoles. V [1]. Structure assignment of lH-pyrazol-3- and 5 amines by means of the 1H NMR δ(4-H)-values of their exo-N-toluenesulfonyl derivatives. J. Heterocyclic Chem., 21 (3) 689–695.
8. Backer H. J., and De Jonge J. (1943) Dérivés de la sulfanilamide renfermant l'anneau 1,2,4‐triazol. Recl. Trav. Chim. Pays-Bas., 62 (3) 158–162.
9. Plesniak K., Zarecki A., and Wicha J. (2007) The smiles rearrangement and the Julia-Kocienski olefination reaction. Top. Curr. Chem., 275 (46) 163–250.
10. Plescia S., Agozzino P, and Fabra I. (1977) A facile synthesis of some pyrazolo[1,5-b]-1,2,4-benzothiadiazepin-5(4H)ones-10,10-dioxides. A new ring system. J. Heterocyclic Chem., 14 (8) 1431–1432.
11. Sheldrick G. (2008) A short history of SHELX. Acta Cryst., Sect. A., 64 (Pt 1) 112–122.