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Several of these compounds show a good safety effect against the phytotoxic action of chloroacetanilide herbicides; P. Diel and I. Maier, Eur. Pat. Appl. 143078 (1985); Chem. Abstr., 103, 215544m (1985).
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Several of these compounds show a good safety effect against the phytotoxic action of chloroacetanilide herbicides; P. Diel and I. Maier, Eur. Pat. Appl. 143078 (1985); Chem. Abstr., 103, 215544m (1985).
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T. Kametani, K. Kigasawa, M. Hiiragi, K. Wakisaka, S. Haga, H. Sugi, K. Tanigawa, Y. Suzuki, K. Fukawa, O. Irino, O. Saita, and S. Yamabe, Heterocycles, 16, 1205 (1981); J. G. Allen, F. R. Atherton, M. J. Hall, C. H. Hassall, S. W. Holmes, R. W. Lambert, L. J. Nisbet, and P. S. Ringrose, Nature (London), 272, 56 (1978).
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5
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0000426890
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T. Kametani, K. Kigasawa, M. Hiiragi, K. Wakisaka, S. Haga, H. Sugi, K. Tanigawa, Y. Suzuki, K. Fukawa, O. Irino, O. Saita, and S. Yamabe, Heterocycles, 16, 1205 (1981); J. G. Allen, F. R. Atherton, M. J. Hall, C. H. Hassall, S. W. Holmes, R. W. Lambert, L. J. Nisbet, and P. S. Ringrose, Nature (London), 272, 56 (1978).
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Baraldi, P.G.1
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0036012151
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Lithium perchlorate in diethyl ether has gained importance as a versatile reaction medium for effecting various organic transformations; A. Heydari, R. Baharfar, M. Rezaie, and S. Aslanzadeh, Chem. Lett., 2002, 368.
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12
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0012927799
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note
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P-C = 152 Hz, CH, Cl).
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13
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0012932202
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note
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When a solution of aldehyde and N,N-dimethylhydrazine was treated with trimethylphosphite/trimethylsilyl chloride in diethyl ether at room temperature for 4 h, the corresponding hydrazone was obtained with high yield.
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14
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33947092127
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D. A. Evans, K. M. Hurst, and J. M. Takacs, J. Am. Chem. Soc., 100, 3467 (1978); Y. Okamoto, T. Azuhata, and H. Sakurai, Chem. Lett., 1981, 1265; Y. Okamoto and H. Sakurai, Synthesis, 1982, 497.
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D. A. Evans, K. M. Hurst, and J. M. Takacs, J. Am. Chem. Soc., 100, 3467 (1978); Y. Okamoto, T. Azuhata, and H. Sakurai, Chem. Lett., 1981, 1265; Y. Okamoto and H. Sakurai, Synthesis, 1982, 497.
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J. E. Franz, U. S. Patent 4084953; Chem. Abst., 89, 109961, (1978); R. Huber, A. Knierzinger, J.-P. Obrecht, and A. Vasella, Helv. Chim. Acta, 68, 1730 (1985); R. Huber and A. Vasella, Helv. Chim. Acta, 70, 1461 (1987); R. Huber and A. Vasella, Tetrahedron, 46, 33 (1990).
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J. E. Franz, U. S. Patent 4084953; Chem. Abst., 89, 109961, (1978); R. Huber, A. Knierzinger, J.-P. Obrecht, and A. Vasella, Helv. Chim. Acta, 68, 1730 (1985); R. Huber and A. Vasella, Helv. Chim. Acta, 70, 1461 (1987); R. Huber and A. Vasella, Tetrahedron, 46, 33 (1990).
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J. E. Franz, U. S. Patent 4084953; Chem. Abst., 89, 109961, (1978); R. Huber, A. Knierzinger, J.-P. Obrecht, and A. Vasella, Helv. Chim. Acta, 68, 1730 (1985); R. Huber and A. Vasella, Helv. Chim. Acta, 70, 1461 (1987); R. Huber and A. Vasella, Tetrahedron, 46, 33 (1990).
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J. E. Franz, U. S. Patent 4084953; Chem. Abst., 89, 109961, (1978); R. Huber, A. Knierzinger, J.-P. Obrecht, and A. Vasella, Helv. Chim. Acta, 68, 1730 (1985); R. Huber and A. Vasella, Helv. Chim. Acta, 70, 1461 (1987); R. Huber and A. Vasella, Tetrahedron, 46, 33 (1990).
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