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Examples of the fused rings include benzene, 1,2,5-thiadiazole, dithiin, benzo[1,4]dithiin, naphtho[1,4]dithiin, furan, thiophene, selenophene, pyrrole, and pyrazine. About Recent Studies, See for Example: (a) Jigami, T.; Takimiya, K.; Aso, Y.; Otsubo, T. Chem. Lett. 1997, 1091;
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18
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85038135812
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note
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Even the selenolate which was obtained in a similar manner hardly afforded the desired selenide (3% yield). In contrast, the reaction of the thiolate with ethyl bromoacetate was found to give the corresponding sulfide in 90% yield. Thus, the low yield in the case of bromoacetaldehyde diethyl ketal can be ascribed to the low reactivity of the substrate.
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19
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85038139750
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note
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7: 377.8464; found: 377.8473.
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21
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0001337056
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(c) Nakazaki, J.; Matsushita, M. M.; Izuoka, A.; Sugawara, T. Tetrahedron Lett. 1999, 40, 5027.
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25
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85038146848
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note
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4-PhCN solution, scanned 200 mV/s).
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26
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85038130734
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and references cited therein
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As to the preparation of charge transfer complexes with amine-based radical donors, see: Sakurai, H.; Izuoka, A.; Sugawara, T. Mol. Cryst. Liq. Cryst. 1997, 306, 879, and references cited therein.
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Sakurai, H.1
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Sugawara, T.3
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