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(a) Joule, J. A.; Mills, K. Heterocyclic Chemistry, 4th ed.; Blackwell Science Ltd.: Cambridge, MA, 2000; pp 194-232.
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Joule, J.A.1
Mills, K.2
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33947473659
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For selected papers for the pyrimidine synthesis via path a, see: (a) Taylor, E. C.; Knoff, R. J.; Meyer, R. F.; Holmes, A.; Hoefle, M. L. J. Am. Chem. Soc. 1960, 82, 5711.
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Taylor, E.C.1
Knoff, R.J.2
Meyer, R.F.3
Holmes, A.4
Hoefle, M.L.5
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4
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(b) Inoue, S.; Saggiomo, A. J.; Nodiff, E. A. J. Org. Chem. 1961, 26, 4504.
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Inoue, S.1
Saggiomo, A.J.2
Nodiff, E.A.3
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5
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84981750720
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(c) Bredereck, H.; Effenberger, F.; Botsch, H.; Rehn, H. Chem. Ber. 1965, 98, 1081.
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Chem. Ber.
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Bredereck, H.1
Effenberger, F.2
Botsch, H.3
Rehn, H.4
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8
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(f) Potts, K. T.; Cipullo, M. J.; Ralli, P.; Theodoridis, G. J. Org. Chem. 1983, 48, 4841.
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Potts, K.T.1
Cipullo, M.J.2
Ralli, P.3
Theodoridis, G.4
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(h) Schenone, P.; Sansebastiano, L.; Mosti, L. J. Heterocycl. Chem. 1990, 27, 295.
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Schenone, P.1
Sansebastiano, L.2
Mosti, L.3
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12
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0029873426
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(j) Yamanaka, H.; Takekawa, T.; Morita, K.; Ishihara, T.; Gupton, J. T. Tetrahedron Lett. 1996, 37, 1829.
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Tetrahedron Lett.
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Yamanaka, H.1
Takekawa, T.2
Morita, K.3
Ishihara, T.4
Gupton, J.T.5
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15
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0013526110
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For selected papers on pyrimidine synthesis via path b, see: Eilingfeld, H.; Patsch, M.; Scheuermann, H. Chem. Ber. 1968, 101, 2426.
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Chem. Ber.
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Eilingfeld, H.1
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(b) Alberola, A.; Andrês, C.; Ortega, A. G.; Pedrosa, R.; Vicente, M. Synth. Commun. 1987, 17, 1309.
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Alberola, A.1
Andrês, C.2
Ortega, A.G.3
Pedrosa, R.4
Vicente, M.5
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18
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0029995229
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For selected papers on pyrimidine synthesis via path d, see: (a) Guzmân, A.; Romero, M.; Talamâs, F. X.; Villena, R.; Greenhouse, R.; Muchowski, J. M. J. Org. Chem. 1996, 61, 2470.
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Guzmân, A.1
Romero, M.2
Talamâs, F.X.3
Villena, R.4
Greenhouse, R.5
Muchowski, J.M.6
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19
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0026692718
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(b) Guzmân, A.; Romero, M.; Talamâs, F. X.; Muchowski, J. M. Tetrahedron Lett. 1992, 24, 3449.
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Tetrahedron Lett.
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Guzmân, A.1
Romero, M.2
Talamâs, F.X.3
Muchowski, J.M.4
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20
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27144523461
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For selected papers on pyrimidine synthesis via path e, see: (a) Pourzal, A.-A. Synthesis 1983, 717.
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Synthesis
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Pourzal, A.-A.1
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21
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11744384546
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(b) Martínez, A. G.; Fernandez, A. H.; Alvarez, R. M.; Losada, M. C. S.; Vilchez, D. M.; Subramanian, L. R.; Hanack, M. Synthesis 1990, 881.
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Synthesis
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Martínez, A.G.1
Fernandez, A.H.2
Alvarez, R.M.3
Losada, M.C.S.4
Vilchez, D.M.5
Subramanian, L.R.6
Hanack, M.7
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22
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(c) Martînez, A. G.; Fernândez, A. H.; Fraile, A. G.; Subramanian, L. R.; Hanack, M. J. Org. Chem. 1992, 57, 1627.
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J. Org. Chem.
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Martînez, A.G.1
Fernândez, A.H.2
Fraile, A.G.3
Subramanian, L.R.4
Hanack, M.5
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23
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0033538080
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(d) Martînez, A. G.; Fernândez, A. H.; Âlvarez, R. M.; Vilchez, M. D. M.; Gutiêrrez, M. L. L.; Subramanian, L. R. Tetrahedron 1999, 55, 4825.
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Tetrahedron
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Martînez, A.G.1
Fernândez, A.H.2
Âlvarez, R.M.3
Vilchez, M.D.M.4
Gutiêrrez, M.L.L.5
Subramanian, L.R.6
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24
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0033106158
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(e) Ghosez, L.; Jnoff, E.; Bayard, P.; Sainte, F.; Beaudegnies, R. Tetrahedron 1999, 55, 3387.
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Tetrahedron
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Ghosez, L.1
Jnoff, E.2
Bayard, P.3
Sainte, F.4
Beaudegnies, R.5
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25
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27144539460
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note
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For example, sets of numbers in 3,4- and 1,6-bond forming reactions shown in Scheme 1 denote the position of bonds formed between N(3)-C(4) and N(1)-C(6).
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27
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2942585558
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(b) Mangelinckx, S.; Giubellina, N.; Kimpe, N. D. Chem. Rev. 2004, 104, 2353.
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Chem. Rev.
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Mangelinckx, S.1
Giubellina, N.2
Kimpe, N.D.3
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29
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33746471983
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(b) Konakahara, T.; Watanabe, A.; Maehara, K.; Nagata, M.; Hojahmat, M. Heterocycles 1993, 35, 1171.
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Heterocycles
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Konakahara, T.1
Watanabe, A.2
Maehara, K.3
Nagata, M.4
Hojahmat, M.5
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30
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0001013495
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(c) Konakahara, T.; Mojahmat, M.; Sujimoto, K. Heterocycles 1997, 45, 271.
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Heterocycles
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Konakahara, T.1
Mojahmat, M.2
Sujimoto, K.3
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31
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0001773607
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(d) Konakahara, T.; Hojahmat, M.; Tamura, S. J. Chem. Soc., Perkin Trans. 1 1999, 2803.
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J. Chem. Soc., Perkin Trans. 1
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Konakahara, T.1
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Tamura, S.3
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0034163796
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(e) Hojahmat, M.; Konakahara, T.; Tamura, S. Heterocycles 2000, 53, 629.
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Heterocycles
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Hojahmat, M.1
Konakahara, T.2
Tamura, S.3
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(f) Konakahara, T.; Ogawa, R.; Tamura, S.; Kakehi, A.; Sakai, N. Heterocycles 2001, 55, 1737.
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Heterocycles
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Konakahara, T.1
Ogawa, R.2
Tamura, S.3
Kakehi, A.4
Sakai, N.5
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34
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(g) Konakahara, T.; Sugama, N.; Yamada, A.; Kakehi, A.; Sakai, N. Heterocycles 2001, 55, 313.
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Heterocycles
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Konakahara, T.1
Sugama, N.2
Yamada, A.3
Kakehi, A.4
Sakai, N.5
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35
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27144506159
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note
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2, were not effective for the reaction.
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36
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27144554139
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note
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9a namely, the existence of the ring affects an easy preparation of this type of a vinyl amidine derivative. Actually, the reaction of the 1-azaallyl anion having a pyridine ring instead of the isoxazole ring with 2-cyanopyrazine did not produce the corresponding vinyl amidine in a practical yield (<10%). Although the reaction of a vinyl amidine involving other aromatic rings with an acetal was not examined, the reaction would proceed. The detailed results will be published elsewhere.
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0242267899
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(a) Gangjee, A.; Adair, O. O.; Queener, S. F. J. Med. Chem. 2003, 46, 5074.
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0242607609
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(b) Perner, R. J.; Gu, Y.-G.; Lee, C.-H.; Bayburt, E. K.; McKie, J.; Alexander, K. M.; Kohlhaas, K. L.; Wismer, C. T.; Mikusa, J.; Jarvis, M. F.; Kowaluk, E. A.; Bhagwat, S. S. J. Med. Chem. 2003, 46, 5249.
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Perner, R.J.1
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(c) Sanmartîn, C.; Echeverrîa, M.; Mendîvil, B.; Cordeu, L.; Cubedo, E.; Garcîa-Foncillas, J.; Font, M.; Palop, J. A. Bioorg. Med. Chem. 2005, 13, 2031.
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Sanmartîn, C.1
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