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(a) Domínguez, E.; Martínez de Marigorta, E.; San Martín, R. Tetrahedron 1994, 50, 2255-2264.
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0001952923
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(b) Domínguez, E.; Martínez de Marigorta, E.; San Martín, R.; Olivera, R. Synlett 1995, 955-956.
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84943418328
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(a) Martin, J. C.; Barton, K. R.; Gott, P. G.; Meen, R. M. J. Org. Chem. 1966, 31, 943-946.
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(a) Abu-Shanab, F. A.; Redhouse, A. D.; Thompson, J. R.; Wakefield, B. J. Synthesis 1995, 557-560.
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(a) Baraldi, P. G.; Barco, A.; Benetti, S.; Pollini, G. P.; Simoni, D. Synthesis 1987, 857-869.
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(a) A review on the Ullmann reaction: Fanta, P. E. Synthesis 1974, 9-21.
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Fanta, P.E.1
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Other examples of the Ullmann reaction: (a) Lindsten, G.; Wennerstrom, O.; Isaksson, R. J. Org. Chem. 1987, 52, 547-554. (b) Matsumoto, H.; Inaba, S.; Rieke, R. D. J. Org. Chem. 1983, 48, 840-843. (c) Tsou, T. T.; Kochi, J. K. J. Am. Chem. Soc. 1979, 101, 7547-7560. (d) Takagi, K.; Hayama, M.; Inokawa, S. Chem. Lett. 1979, 917-918. (e) Bamfield, P.; Quan, P. M. Synthesis 1978, 537-538.
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Other examples of the Ullmann reaction: (a) Lindsten, G.; Wennerstrom, O.; Isaksson, R. J. Org. Chem. 1987, 52, 547-554. (b) Matsumoto, H.; Inaba, S.; Rieke, R. D. J. Org. Chem. 1983, 48, 840-843. (c) Tsou, T. T.; Kochi, J. K. J. Am. Chem. Soc. 1979, 101, 7547-7560. (d) Takagi, K.; Hayama, M.; Inokawa, S. Chem. Lett. 1979, 917-918. (e) Bamfield, P.; Quan, P. M. Synthesis 1978, 537-538.
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Other examples of the Ullmann reaction: (a) Lindsten, G.; Wennerstrom, O.; Isaksson, R. J. Org. Chem. 1987, 52, 547-554. (b) Matsumoto, H.; Inaba, S.; Rieke, R. D. J. Org. Chem. 1983, 48, 840-843. (c) Tsou, T. T.; Kochi, J. K. J. Am. Chem. Soc. 1979, 101, 7547-7560. (d) Takagi, K.; Hayama, M.; Inokawa, S. Chem. Lett. 1979, 917-918. (e) Bamfield, P.; Quan, P. M. Synthesis 1978, 537-538.
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Tsou, T.T.1
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Other examples of the Ullmann reaction: (a) Lindsten, G.; Wennerstrom, O.; Isaksson, R. J. Org. Chem. 1987, 52, 547-554. (b) Matsumoto, H.; Inaba, S.; Rieke, R. D. J. Org. Chem. 1983, 48, 840-843. (c) Tsou, T. T.; Kochi, J. K. J. Am. Chem. Soc. 1979, 101, 7547-7560. (d) Takagi, K.; Hayama, M.; Inokawa, S. Chem. Lett. 1979, 917-918. (e) Bamfield, P.; Quan, P. M. Synthesis 1978, 537-538.
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Takagi, K.1
Hayama, M.2
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23
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85024471340
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Other examples of the Ullmann reaction: (a) Lindsten, G.; Wennerstrom, O.; Isaksson, R. J. Org. Chem. 1987, 52, 547-554. (b) Matsumoto, H.; Inaba, S.; Rieke, R. D. J. Org. Chem. 1983, 48, 840-843. (c) Tsou, T. T.; Kochi, J. K. J. Am. Chem. Soc. 1979, 101, 7547-7560. (d) Takagi, K.; Hayama, M.; Inokawa, S. Chem. Lett. 1979, 917-918. (e) Bamfield, P.; Quan, P. M. Synthesis 1978, 537-538.
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Bamfield, P.1
Quan, P.M.2
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24
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84942183942
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A very recent diaryl synthesis through Suzuki methodology: (a) Anderson J. C.; Namli, H. Synlett 1995, 765-766. Other papers on Suzuki reaction: (b) Watanabe, T.; Miyaura, N.; Suzuki, A. Synlett 1992, 207-210. (c) Suzuki, A. Pure Appl. Chem. 1994, 213-222.
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A very recent diaryl synthesis through Suzuki methodology: (a) Anderson J. C.; Namli, H. Synlett 1995, 765-766. Other papers on Suzuki reaction: (b) Watanabe, T.; Miyaura, N.; Suzuki, A. Synlett 1992, 207-210. (c) Suzuki, A. Pure Appl. Chem. 1994, 213-222.
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A very recent diaryl synthesis through Suzuki methodology: (a) Anderson J. C.; Namli, H. Synlett 1995, 765-766. Other papers on Suzuki reaction: (b) Watanabe, T.; Miyaura, N.; Suzuki, A. Synlett 1992, 207-210. (c) Suzuki, A. Pure Appl. Chem. 1994, 213-222.
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note
-
Similarly to some other isoxazolium salts of the literature (see ref 23), 6a turned yellow and decomposed in 1-2 months at room temperature.
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