Reactions of 4(6)-chloro-5-nitropyrimidines with nucleophilic agents (review)
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Organic Chemistry Nucleophilic Agent
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- 1.Zh. N. Aksel'rod and V. M. Berezovskii, Usp. Khim.,39, No. 8, 1337–1368 (1970).Google Scholar
- 2.T. G. Arutyunyan, M. P. Nemeryuk, and N. I. Traven', Khim. Geterotsikl. Soedin., No. 2, 258–264 (1989).Google Scholar
- 3.I. V. Boldyrev, O. M. Polumbrik, and L. N. Markovskii, ibid., No. 11, 1545–1549 (1980).Google Scholar
- 4.I. V. Boldyrev, I. F. Vladimirtsev, V. P. Borisenko, et al., Fiziol. Aktiv. Veshchestva, No. 14, 80–84 (1982).Google Scholar
- 5.V. I. Drozd and V. N. Knyazev, Izv. Sibirsk. Otd. Akad. Nauk SSSR, Ser. Khim. Nauk, No. 9, 52–65 (1987).Google Scholar
- 6.M. P. Nemeryuk, A. L. Sedov, V. A. Makarov, et al., Khim. Geterotsikl. Soedin., No. 10, 999–1000 (1991).Google Scholar
- 7.G. Ya. Remennikov and V. M. Cherkasov, Ukr. Khim. Zh.,51, No. 3, 313–316 (1985).Google Scholar
- 8.V. L. Rusinov, A. Yu. Petrov, and O. N. Chupakhin, Khim. Geterotsikl. Soedin., No. 2, 147–165 (1985).Google Scholar
- 9.A. L. Sedov, V. A. Makarov, M. P. Nemeryuk, et al., Summaries of Papers Presented at the 5th Moscow Conference on Organic Chemistry and Technology [in Russian], Moscow (1989), p. 229.Google Scholar
- 10.A. L. Sedov, V. A. Makarov, M. P. Nemeryuk, et al., Summaries of Papers Presented at the 2nd All-Union Conference on the Chemistry of Enamines [in Russian], Perm (1991), p. 17.Google Scholar
- 11.Yu. L. Yagupol'skii, M. T. Kolychev, and V. M. Cherkasov, Khim. Geterotsikl. Soedin., No. 5, 710–711 (1986).Google Scholar
- 12.E. S. Ahmed, E. B. Pederson, and C. M. Nielsen, Chem. Scripta,29, No. 4, 379–382 (1989).Google Scholar
- 13.M. E. C. Biffin, D. J. Broun, and Q. N. Porter, J. Chem. Soc. (C), No. 8, 2159–2162 (1968).Google Scholar
- 14.M. E. C. Biffin, D. J. Broun, and Q. N. Porter, ibid., No. 17, 2162–2164.Google Scholar
- 15.M. Bimmer, P. Langen, and H. Plaul, West German Patent No. 221,736; Chem. Abstr.,104, N 68,880h (1982).Google Scholar
- 16.D. J. Broun, The Pyrimidines, New York (1962), pp. 138–156.Google Scholar
- 17.D. J. Broun, F. W. Ford, and M. N. Paddon-Pow, J. Chem. Soc. (C), No. 12, 1452–1454 (1968).Google Scholar
- 18.D. J. Broun, The Pyrimidines. Supplement I, New York (1970), pp. 94–109.Google Scholar
- 19.J. D. Chesney and M. Gonzales-Sierra, Pharm. Res., 146–147 (1985).Google Scholar
- 20.B. E. Christensen, Q. Stahl, and F. Lehmkuhl, J. Org. Chem.,36, No. 11, 2462–2466 (1971).Google Scholar
- 21.A. G. Ciba-Geigy, Austrian Patent No. 327,605; Chem. Abstr.,85, N 29,570b (1976).Google Scholar
- 22.J. Clark, I. Gelling, and G. Neath, Chem. Commun.,17, 859–860 (1967).Google Scholar
- 23.J. Clark, I. Gelling, I. W. Sounthon, et al., J. Chem. Soc. (C), No. 3, 494–498 (1970).Google Scholar
- 24.J. Clark, B. Parvizi, and I. W. Sounthon, J. Chem. Soc., Perkin I, No. 2, 125–130 (1976).Google Scholar
- 25.J. Clark, B. Parvizi, and R. Colman, ibid., No. 9, 1004–1007.Google Scholar
- 26.T. L. Cupps, D. S. Wise, and L. B. Townsend, J. Org. Chem.,48, 1060–1064 (1983).Google Scholar
- 27.M. H. Elnagoli, F. M. Abdel-Calil, and B. Y. Riad, Heterocycles,20, No. 12, 2437–2470 (1983).Google Scholar
- 28.H. P. Ficher, West German Patent No. 2,223,644; Chem. Abstr.,78, N 43,506x (1973).Google Scholar
- 29.H. P. Ficher, West German Patent No. 2,356,644; Chem. Abstr.,82, N 27,230e (1974).Google Scholar
- 30.H. P. Ficher, West German Patent No. 2,520,381; Chem. Abstr.,84, N 74,306k (1976).Google Scholar
- 31.H. P. Ficher, Australian Patent No. 42,126; Chem. Abstr.,89, N 215,426 (1984).Google Scholar
- 32.A. E. Frissen, A. T. M. Marcelis, and G. Ceurtsen, Tetrahedron,45, No. 16, 5151–5162 (1986).Google Scholar
- 33.S. Gregson and G. Shaw, J. Chem. Soc., Perkin Trans., No. 1, 187–190 (1985).Google Scholar
- 34.M. R. Harnden and D. T. Hurst, Austral. J. Chem.,43, No. 1, 47–53 (1990).Google Scholar
- 35.R. Hull, J. Chem. Soc., No. 2, 481–484 (1959).Google Scholar
- 36.D. T. Hurst, C. Beaument, D. T. E. Jones, et al., Australian J. Chem.,41, No. 8, 1209–1219 (1988).Google Scholar
- 37.T. Kamikawa, S. Fujie, Y. Yamagiwa, et al., Chem. Commun., No. 3, 195–196 (1988).Google Scholar
- 38.T. Kishimoto, K. Ishimitsu, and T. Yamada, British Patent No. 9,005,134; Chem. Abstr.,113, N 132,210e (1990).Google Scholar
- 39.H. E. Kleine-Natrop, Acta ALlerg. (Kbh.),21, No. 4, 319–328 (1966).Google Scholar
- 40.H. Kosaki, Y. Kitade, S. Senda, et al., J. Org. Chem.,46, 846–849 (1981).Google Scholar
- 41.H. Kosaki, Y. Kitade, H. Sajiki, et al., Tetrahedron Lett.,27, No. 28, 3263–3266 (1986).Google Scholar
- 42.D. L. Ladd, US Patent No. 4,336,255; Chem. Abstr., N 98,377d (1982).Google Scholar
- 43.O. W. Lever and B. R. Vestal, J. Heterocycl. Chem.,23, 901–902 (1986).Google Scholar
- 44.A. T. M. Marcelis and H. C. Van der Plas, Tetrahedron,45, No. 9, 2693–2702 (1989).Google Scholar
- 45.E. Mulliez, Tetrahedron Lett.,30, No. 45, 6169–6172 (1989).Google Scholar
- 46.B. Narr, J. Roch, E. Mueller, et al., West German Patent No. 2,341,925; Chem. Abstr.,83, N 43,369h (1975).Google Scholar
- 47.H. C. Van der Plas and H. Jongejan, Tetrahedron Lett.,8, No. 44, 4385–4388 (1967).Google Scholar
- 48.H. C. Van der Plas, H. Jongejan, and A. Koudijs, J. Heterocycl. Chem.,15, No. 3, 485–487 (1978).Google Scholar
- 49.H. C. Van der Plas and H. Jongejan, Tetrahedron Lett.,23, No. 38, 3965–3968 (1982).Google Scholar
- 50.H. C. Van der Plas, V. N. Charushin, and B. Valdhuizen, J. Org. Chem.,48, 1354–1357 (1983).Google Scholar
- 51.J. H. Ridd, Z. Chem.,6, 201–206 (1968).Google Scholar
- 52.H. F. Rihald, European Patent No. 366,085.Google Scholar
- 53.O. Rousseaux, D. Blondeau, and H. Sliwa, Heterocycles,31, No. 2, 277–281 (1990).Google Scholar
- 54.T. L. Su, K. A. Watanbe, and J. J. Fox, Tetrahedron,38, No. 8, 1405–1408 (1982).Google Scholar
- 55.E. C. Taylor and E. E. Gareia, J. Org. Chem.,29, No. 8, 2121–2124 (1964).Google Scholar
- 56.G. Tennaut and G. M. Wallace, J. Chem. Soc., Chem. Commun., No. 4, 267–268 (1982).Google Scholar
- 57.K. A. Watanabe, T. L. Su, K. W. Paukiwier, et al., Heterocycles,21, No. 1, 289–301 (1984).Google Scholar
- 58.H. Zondler, H. S. Forrest, and J. M. Lagowski, J. Heterocycl. Chem.,4, 675–678 (1967).Google Scholar
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