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1
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0012814523
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ed by K. T. Potts, Pergamon, Oxford, Chap. 4.30;
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A. J. Elliott, in "Comprehensive Heterocyclic Chemistry," ed by K. T. Potts, Pergamon, Oxford (1984), Vol. 6, Chap. 4.30; R. A. Aitken and L. Hill, in "Comprehensive Heterocyclic Chemistry II," ed by I. Shinkai, Pergamon, Oxford (1996), Vol. 3, Chap. 3.09.
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Comprehensive Heterocyclic Chemistry
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Elliott, A.J.1
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2
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0012858240
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ed by I. Shinkai, Pergamon, Oxford, Chap. 3.09
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A. J. Elliott, in "Comprehensive Heterocyclic Chemistry," ed by K. T. Potts, Pergamon, Oxford (1984), Vol. 6, Chap. 4.30; R. A. Aitken and L. Hill, in "Comprehensive Heterocyclic Chemistry II," ed by I. Shinkai, Pergamon, Oxford (1996), Vol. 3, Chap. 3.09.
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Comprehensive Heterocyclic Chemistry II
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Aitken, R.A.1
Hill, L.2
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3
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0012875220
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K. T. Tanatarova and K. B. Erzhanov, Deposited doc., VINITI 3428 (1979)
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K. T. Tanatarova and K. B. Erzhanov, Deposited doc., VINITI 3428 (1979); Chem. Abstr., 94, 191604y (1981). The authors elucidated structure of the product only by IR data and elemental analysis results of chlorine and sulfur (analyses of carbon and hydrogen were not reported). The reported mp 94-95°C of 1a does not agree with mp 68°C of our sample of 1a, but agrees with mp 95-96°C of our sample of 2a. The reported IR data also agree with those of 2a rather than those of 1a.
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-
-
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4
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4244077577
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K. T. Tanatarova and K. B. Erzhanov, Deposited doc., VINITI 3428 (1979); Chem. Abstr., 94, 191604y (1981). The authors elucidated structure of the product only by IR data and elemental analysis results of chlorine and sulfur (analyses of carbon and hydrogen were not reported). The reported mp 94-95°C of 1a does not agree with mp 68°C of our sample of 1a, but agrees with mp 95-96°C of our sample of 2a. The reported IR data also agree with those of 2a rather than those of 1a.
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(1981)
Chem. Abstr.
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-
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5
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0012857348
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G. W. Astrologes and J. C. Martin, J. Am. Chem. Soc., 95, 6909 (1973). Tropone- and tropothione-annulated 5-oxo derivatives are known as antibiotic; S. Tsubotani, Y. Wada, K. Kamiya, H. Okazaki, and S. Harada, Tetrahedron Lett., 25, 419 (1984).
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J. Am. Chem. Soc.
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Astrologes, G.W.1
Martin, J.C.2
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6
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0021349380
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G. W. Astrologes and J. C. Martin, J. Am. Chem. Soc., 95, 6909 (1973). Tropone- and tropothione-annulated 5-oxo derivatives are known as antibiotic; S. Tsubotani, Y. Wada, K. Kamiya, H. Okazaki, and S. Harada, Tetrahedron Lett., 25, 419 (1984).
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Tetrahedron Lett.
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Tsubotani, S.1
Wada, Y.2
Kamiya, K.3
Okazaki, H.4
Harada, S.5
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7
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0012810166
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a) M. A. Torosyan, R. S. Mirzoyan, S. S. Isakhanyan, and A. M. Arutynyan, Ann. Khim. Zh., 39, 124 (1986); Chem. Abstr., 106, 138299t (1987).
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Torosyan, M.A.1
Mirzoyan, R.S.2
Isakhanyan, S.S.3
Arutynyan, A.M.4
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8
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-
4243928081
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a) M. A. Torosyan, R. S. Mirzoyan, S. S. Isakhanyan, and A. M. Arutynyan, Ann. Khim. Zh., 39, 124 (1986); Chem. Abstr., 106, 138299t (1987).
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Chem. Abstr.
, vol.106
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9
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0012896131
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b) E. Thoumazeau, B. Jousseaume, F. Tiffon, and J. G. Duboudin, Heterocycles, 19, 637 (1982).
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Thoumazeau, E.1
Jousseaume, B.2
Tiffon, F.3
Duboudin, J.G.4
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11
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0001153050
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d) J. F. King, P. de Mayo, C. L. McIntosh, K. Piers, and D. J. H. Smith, Can. J. Chem., 48, 3704 (1970).
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King, J.F.1
De Mayo, P.2
McIntosh, C.L.3
Piers, K.4
Smith, D.J.H.5
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12
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0001353068
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A. W. M. Lee, W. H. Chan, L. S. Jiang, and K. W. Poon, J. Chem. Soc., Chem. Commun., 1997, 611.
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J. Chem. Soc., Chem. Commun.
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Lee, A.W.M.1
Chan, W.H.2
Jiang, L.S.3
Poon, K.W.4
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13
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0030482396
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For preparation of stable sulfenic acids, see: a) A. Ishii, K. Komiya, and J. Nakayama, J. Am. Chem. Soc., 118, 12836 (1996).
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J. Am. Chem. Soc.
, vol.118
, pp. 12836
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Ishii, A.1
Komiya, K.2
Nakayama, J.3
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14
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0030894735
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and references therein
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b) K. Goto, M. Holler, and R. Okazaki, J. Am. Chem. Soc., 119, 1460 (1997), and references therein.
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Goto, K.1
Holler, M.2
Okazaki, R.3
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15
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0003928002
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ed by S. V. Ley, Pergamon, Oxford, Chap. 2.03
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P. C. B. Page, R. D. Wilkes, and D. Reynolds, in "Comprehensive Organic Functional Group Transformations," ed by S. V. Ley, Pergamon, Oxford (1995), Vol. 2, Chap. 2.03.
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Page, P.C.B.1
Wilkes, R.D.2
Reynolds, D.3
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16
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0034699845
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a) J. Nakayama, K. Takahashi, T. Watanabe, Y. Sugihara, and A. Ishii, Tetrahedron Lett., 41, 8349 (2000).
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Tetrahedron Lett.
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Nakayama, J.1
Takahashi, K.2
Watanabe, T.3
Sugihara, Y.4
Ishii, A.5
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17
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0035844642
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b) J. Nakayama, K. Takahashi, Y. Sugihara, and A. Ishii, Tetrahedron Lett., 42, 4017 (2001).
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Tetrahedron Lett.
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Nakayama, J.1
Takahashi, K.2
Sugihara, Y.3
Ishii, A.4
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18
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0036337902
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c) J. Nakayama, K. Takahashi, Y. Ono, M. Morita, Y. Sugihara, and A. Ishii, Heteroatom Chem., 13, 424 (2002).
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Nakayama, J.1
Takahashi, K.2
Ono, Y.3
Morita, M.4
Sugihara, Y.5
Ishii, A.6
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20
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0000002499
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ed by E. Winterfeldt, Pergamon, Oxford, Chap. 4.6, and references cited therein
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Bruckner, R. in "Comprehensive Organic Synthesis," ed by E. Winterfeldt, Pergamon, Oxford (1991), Vol. 6, Chap. 4.6, and references cited therein.
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Comprehensive Organic Synthesis
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Bruckner, R.1
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21
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84890652880
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R. C. de Laet, A. J. J. M. van Breemen, A. J. Derksen, M. van Klaveren, and B. Zwanenburg, Phosphorus, Sulfur, Silicon, 74, 371 (1993).
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Phosphorus, Sulfur, Silicon
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De Laet, R.C.1
Van Breemen, A.J.J.M.2
Derksen, A.J.3
Van Klaveren, M.4
Zwanenburg, B.5
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22
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0012881243
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-
note
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We cannot rule out the possibility that 11 is formed through ring-opening of sulfoxide 12.
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