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more..
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26
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33845551515
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For a preparation of diselenohydroquinone dilithiumsalt see also
-
For a preparation of diselenohydroquinone dilithiumsalt see also Tiecco, M.; Testaferri, L.; Tingoli, M.; Chianelli, D.; Montanucci, M. J. Org. Chem. 1983, 48, 4289.
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31
-
-
85030577837
-
-
note
-
The yield of crude product precipitated directly from the reaction mixture was 63%, sufficiently pure for synthetic applications.
-
-
-
-
32
-
-
85030583697
-
-
note
-
Technical quality; unsuccessful recrystallisation attempts; pure enough for synthetic applications viz. as precursor for the bis(2-thienylseleno) compound.
-
-
-
-
35
-
-
85030580533
-
-
note
-
Recrystallisation from ethanol/water (1:1).
-
-
-
-
36
-
-
0028122568
-
-
Tiecco, M.; Testaferri, L.; Tingoli, M.; Marini, F.; Mariggio, S. Tetrahedron 1994, 50, 10549.
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(1994)
Tetrahedron
, vol.50
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Tiecco, M.1
Testaferri, L.2
Tingoli, M.3
Marini, F.4
Mariggio, S.5
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37
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0000823336
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Greenberg, B.; Gould, E. S.; Burlant, W. J. Am. Chem. Soc. 1956, 78, 4028.
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39
-
-
85030583630
-
-
note
-
Even with a limiting amount of 6a no bis-selenylated product appeared according to TLC, GCeMS and NMR.
-
-
-
-
40
-
-
85030580659
-
-
note
-
A 100-fold excess of 4a was employed to obtain 9j, 9k and 9l.
-
-
-
-
42
-
-
85030587672
-
-
note
-
+, 46), 239(100), 206(9), 158 (37)] were isolable by bulb-to-bulb distillation (220 °C air-bath, 1 mmHg).
-
-
-
-
43
-
-
1542404490
-
-
Vvedenskii, V. Y.; Zinchenko, S. V.; Sthefan, E. D.; Ulyev, M. V.; Zhnikin, A. R.; Shkarupa, T. A.; Deryagina, E. N. Sulfur Lett. 1992, 14, 129.
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Vvedenskii, V.Y.1
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Zhnikin, A.R.5
Shkarupa, T.A.6
Deryagina, E.N.7
-
44
-
-
85030578036
-
-
note
-
Active coal needed to remove polymer material.
-
-
-
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