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7
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Dias A.R., Martins A.M., Ascenso J.R., Ferreira H., Duarte M.T., and Henriques R.T. Inorg. Chem. 42 (2003) 2675
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14
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4644311919
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Yoshida Y., Mohri J., Ishii S., Mitani M., Saito J., Matsui S., Makio H., Nakano T., Tanaka H., Onda M., Yamamoto Y., Mizuno A., and Fujita T. J. Am. Chem. Soc. 126 (2004) 12023
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16
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33748401992
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Rogers A.J., Solari E., Floriani C., Chiesi-Villa A., and Rizzoli C. J. Chem. Soc., Dalton Trans. (1997) 2385
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Chiesi-Villa, A.4
Rizzoli, C.5
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18
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0001312097
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Giannini L., Solari E., De Angelis S., Ward T.R., Floriani C., Chiesi-Villa A., and Rizzoli C. J. Am. Chem. Soc. 117 (1995) 5801
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Chiesi-Villa, A.6
Rizzoli, C.7
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20
-
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0001970356
-
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Royal G., Dahaoui-Gindrey V., Dahaoui S., Tabard A., Guilard R., Pullumbi P., and Lecomte C. Eur. J. Org. Chem. (1998) 1971
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Tabard, A.4
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Pullumbi, P.6
Lecomte, C.7
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21
-
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52949124405
-
-
note
-
0.2: C, 77.63; H, 11.08; N, 9.01. Found: C, 77.80; H, 11.62; N, 8.66.
-
-
-
-
23
-
-
2342662623
-
-
Karame I., Jahjah M., Messaoudi A., Tommasino M.L., and Lemaire M. Tetrahedron: Asymmetry 15 (2004) 1569
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-
Karame, I.1
Jahjah, M.2
Messaoudi, A.3
Tommasino, M.L.4
Lemaire, M.5
-
25
-
-
52949124787
-
-
note
-
2: C, 71.09; H, 10.07; N, 10.36. Found: C, 71.20; H, 9.82; N, 13.78.
-
-
-
-
26
-
-
33746281731
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Munhá R.F., Namorado S., Barroso S., Duarte M.T., Ascenso J.R., Dias A.R., and Martins A.M. J. Organomet. Chem. 691 (2006) 3853
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J. Organomet. Chem.
, vol.691
, pp. 3853
-
-
Munhá, R.F.1
Namorado, S.2
Barroso, S.3
Duarte, M.T.4
Ascenso, J.R.5
Dias, A.R.6
Martins, A.M.7
-
27
-
-
52949096473
-
-
note
-
2 = 0.1476.
-
-
-
-
29
-
-
52949112991
-
-
note
-
2 (1.10 g, 2.3 mmol). A reflux condenser was adapted and the reaction mixture was left under mild reflux. After 3 h, 90% of the THF was evaporated. The remaining THF was filtered and the bright yellow solid was rinsed with hexanes and taken to dryness (1.06 g, 87%).
-
-
-
-
30
-
-
52949128337
-
-
note
-
2): C, 57.93; H, 8.06; N, 6.59. Found: C, 58.73; H, 8.99; N, 6.56.
-
-
-
-
31
-
-
52949122106
-
-
note
-
2 = 0.1055.
-
-
-
-
32
-
-
52949118460
-
-
note
-
3COOH). The solution was evaporated, the polymer was precipitated by addition of water and dried in a vacuum desiccator during two days.
-
-
-
-
33
-
-
0024092618
-
-
The polymerization mixture was quenched with acidic methanol (2% HCl) and the polymer was filtered, washed with methanol and dried in a vacuum oven at 60 °C during two days.
-
Chien J.C.W., and Wang B.-P. J. Polym. Sci., Part A: Polym. Chem. 26 (1988) 3089 The polymerization mixture was quenched with acidic methanol (2% HCl) and the polymer was filtered, washed with methanol and dried in a vacuum oven at 60 °C during two days.
-
(1988)
J. Polym. Sci., Part A: Polym. Chem.
, vol.26
, pp. 3089
-
-
Chien, J.C.W.1
Wang, B.-P.2
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