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26944471241
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note
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2O (150 mL) and hexanes (150 mL). The solid was suspended in benzene (300 mL) at 60 °C for 15 min, allowed to cool, filtered and dried in vacuo to give 4 (31.81 g, 37% yield).
-
-
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31
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0030747607
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0001617170
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0022199809
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These reagents have been used in similar transformations: C. Bilger, P. Demerseman and R. Royer, J. Heterocycl. Chem., 1985, 22, 735.
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35
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26944451748
-
-
note
-
2: C 81.07, H 4.54. Found: C 81.24, H 4.75.
-
-
-
-
36
-
-
26944452513
-
-
note
-
2: C 86.68, H 4.66, N 4.04. Found: C 86.66, H 4.88, N 4.12.
-
-
-
-
37
-
-
26944471409
-
-
note
-
2) = 0.1182 (all data). CCDC 276257. See http://dx.doi.org/10.1039/b508538a for crystallographic data in CIF or other electronic format.
-
-
-
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38
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0001717682
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K. Bernardo, S. Leppard, A. Robert, G. Commenges, F. Dahan and B. Meunier, New J. Chem., 1995, 19, 129;
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39
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0036262856
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-
40
-
-
26944438774
-
-
note
-
2Fe: C 80.43, H 4.05, N 3.75. Found: C 80.73, H 3.80, N 3.57.
-
-
-
-
41
-
-
0038824066
-
-
S. Mizukami, H. Houjou, Y. Nagawa and M. Kanesato, Chem. Commun., 2003, 1148.
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42
-
-
26944472514
-
-
2) = 0.0874 (all data) and Flack = -0.021(8). CCDC 276258. See http://dx.doi.org/10.1039/ b508538a for crystallographic data in CIF or other electronic format.
-
-
-
-
43
-
-
26944503565
-
-
note
-
2) = 0.1642 (all data). CCDC 276259. See http:// dx.doi.org/10.1039/b508538a for crystallographic data in CIF or other electronic format .
-
-
-
|