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R. A. Abramovitch and R. Jcyaraman in 'Azides and Nitrenes,' ed. E. F. V. Scriven, Academic Press, New York, ch. 6
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R. A. Abramovitch and R. Jcyaraman in 'Azides and Nitrenes,' ed. E. F. V. Scriven, Academic Press, New York, 1984, ch. 6.
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2
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M. Novak. L. H. Rovin. M. Pclecanou. J. Mulero, and R. K. Lagerman, and references ciled therein
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5
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33845554688
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(a) R. A. Abramovitch, M. Cooper, S. Iyer, R. Jeyaraman, and J. A. R. Rodrigues.,;
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(a) R. A. Abramovitch, M. Cooper, S. Iyer, R. Jeyaraman, and J. A. R. Rodrigues. J. Org. Chem., 1982, 47, 4819.
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6
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(b) R. A. Abramovitch, Hawi, J. A. R. Rodrigues, and T. R.Trombeta.
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(b) R. A. Abramovitch. A. Hawi, J. A. R. Rodrigues, and T. R.Trombeta. J. Chem. Soc. Chem. Commun., 1986. 283.
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7
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8th IUPAC Conference on Physical Organic Chemistry. Tokyo, Aug
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R. A. Abramovitch, 8th IUPAC Conference on Physical Organic Chemistry. Tokyo, Aug. 24—29, 1986.
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Abramovitch, R.A.1
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8
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R. A. Abramovitch, H. H. Gibson. Jr., and G. Hutlner. 192nd American Chemical Society National Meeting. Anaheim. CA. Abstract No. 300. Sept
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R. A. Abramovitch, H. H. Gibson. Jr., and G. Hutlner. 192nd American Chemical Society National Meeting. Anaheim. CA. Abstract No. 300. Sept. 7—12,' 1986.
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G. Alvernhe. and M. N. Inbasekaran, Tetrahedron Lett
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R. A. Abramovitch, G. Alvernhe. and M. N. Inbasekaran, Tetrahedron Lett., 1977, 1113.
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Abramovitch, R.A.1
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0000394955
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R. A. Abramovitch, G. Alvernhe. N. L. Dassanayake, M. N. Inbaseka- ran, and S. Kato, J. Am. Chem. Soc, 1981, 103, 4558.
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Abramovitch, R.A.1
Alvernhe, G.2
Inbaseka, M.N.3
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37049102510
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A. T. Tomas, J. Chem. Soc, Perkin Trans. 1
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A. R. Katritzky, P. Ballestcros, and A. T. Tomas, J. Chem. Soc, Perkin Trans. 1, 1981, 1495.
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Katritzky, A.R.1
Ballestcros, P.2
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84943028022
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An authentic sample of (6) was prepared from 2.4.6-tri- phenylpyrylium tetrafluoroboratc and A*-acetyl-J>-phenylenedi- aminc and had m.p. 179—180°C.t R. M. Claramunt and J. Elgucro, Collect. Czech. Chem. Commun., re- ported m.p. 169—171 °C for this compound
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An authentic sample of (6) was prepared from 2.4.6-tri- phenylpyrylium tetrafluoroboratc and A*-acetyl-J>-phenylenedi- aminc and had m.p. 179—180°C.t R. M. Claramunt and J. Elgucro, Collect. Czech. Chem. Commun., 1981, 46, 584, re- ported m.p. 169—171 °C for this compound.
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0001498254
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Tetrahedron. 1978, 34, 2723; P. Kovacic and C. Wu
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L.-S. Wen and P. Kovacic, Tetrahedron. 1978, 34, 2723; P. Kovacic and C. Wu, J. Org. Chem. 1961.26, 749.
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Wen, L.-S.1
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J. Roy. and V. Uma. Can
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R. A. Abramovitch, J. Roy. and V. Uma. Can. J. Chem. 1965, 43. 3407.
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D. S. Breslow in 'Nitrenes.' ed. W. Lwowski, Wiley, New York, 1970. ch. 8, p. 271; G. H. Williams. Homolylic Aromatic Substitution,' Pergamon Press, Oxford
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D. S. Breslow in 'Nitrenes.' ed. W. Lwowski, Wiley, New York, 1970. ch. 8, p. 271; G. H. Williams. "Homolylic Aromatic Substitution,' Pergamon Press, Oxford. 1960, pp. 60—67.
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J. March, 'Advanced Organic Chemistry. 2nd edn., McGraw- Hill, New York
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J. March, 'Advanced Organic Chemistry." 2nd edn., McGraw- Hill, New York, 1977, pp. 1063—1066.
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