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0031949091
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For examples: K. Takimiya, A. Oharuda, A. Morikami, Y. Aso, and T. Otsubo, Angew. Chem. Int. Ed., 27, 619 (1998); K. Takimiya, A. Morikami, Y. Aso, and T. Otubo, J. Chem. Soc., Chem. Commun. 1997, 1925; M. R. Bryce, Aldrichmica Acta, 18, 73 (1985).
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J. Chem. Soc., Chem. Commun.
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Otubo, T.4
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For examples: K. Takimiya, A. Oharuda, A. Morikami, Y. Aso, and T. Otsubo, Angew. Chem. Int. Ed., 27, 619 (1998); K. Takimiya, A. Morikami, Y. Aso, and T. Otubo, J. Chem. Soc., Chem. Commun. 1997, 1925; M. R. Bryce, Aldrichmica Acta, 18, 73 (1985).
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Bryce, M.R.1
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Kato, S.1
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0030884252
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S. Kato, T. Komuro, T. Kanda, H. Ishihara, and T. Murai, J. Am. Chem. Soc., 115, 3000 (1993); T. Murai, K. Kakami, A. Hayashi, T. Komuro, H. Takada, M. Fujii, T. Kanda, and S. Kato, J. Am. Chem. Soc., 119, 8592 (1997); T. Murai, H. Takada, K. Kakami, M. Fujii, M. Maeda, and S. Kato, Tetrahedron, 53, 12237 (1997); T. Murai and S. Kato, Sulfur Reports, 20, 397 (1998).
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Murai, T.1
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Fujii, M.6
Kanda, T.7
Kato, S.8
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0030880668
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S. Kato, T. Komuro, T. Kanda, H. Ishihara, and T. Murai, J. Am. Chem. Soc., 115, 3000 (1993); T. Murai, K. Kakami, A. Hayashi, T. Komuro, H. Takada, M. Fujii, T. Kanda, and S. Kato, J. Am. Chem. Soc., 119, 8592 (1997); T. Murai, H. Takada, K. Kakami, M. Fujii, M. Maeda, and S. Kato, Tetrahedron, 53, 12237 (1997); T. Murai and S. Kato, Sulfur Reports, 20, 397 (1998).
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Kato, S.6
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0000265489
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S. Kato, T. Komuro, T. Kanda, H. Ishihara, and T. Murai, J. Am. Chem. Soc., 115, 3000 (1993); T. Murai, K. Kakami, A. Hayashi, T. Komuro, H. Takada, M. Fujii, T. Kanda, and S. Kato, J. Am. Chem. Soc., 119, 8592 (1997); T. Murai, H. Takada, K. Kakami, M. Fujii, M. Maeda, and S. Kato, Tetrahedron, 53, 12237 (1997); T. Murai and S. Kato, Sulfur Reports, 20, 397 (1998).
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0011205599
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Tetrahedron Lett.
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Synthesis
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12
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0009198254
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note
-
3PSe: C, 40.97; H, 5.16%.
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13
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0026679820
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The synthesis and synthetic application of α-phosphoryl selenides are rare: M. Mikolajczyk and W. H. Midura, Tetrahedron Asym., 3, 1515 (1992); C. D. Gabbutt and J. D. Hepworth, "Comprehensive Organic Functional group Transformations," ed by A. R. Katritzky, O. Meth-Cohn, and C. W. Rees, Pergamon, Oxford, UK (1995), Vol. 4, p. 347.
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Tetrahedron Asym.
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Mikolajczyk, M.1
Midura, W.H.2
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14
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0026679820
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ed by A. R. Katritzky, O. Meth-Cohn, and C. W. Rees, Pergamon, Oxford, UK
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The synthesis and synthetic application of α-phosphoryl selenides are rare: M. Mikolajczyk and W. H. Midura, Tetrahedron Asym., 3, 1515 (1992); C. D. Gabbutt and J. D. Hepworth, "Comprehensive Organic Functional group Transformations," ed by A. R. Katritzky, O. Meth-Cohn, and C. W. Rees, Pergamon, Oxford, UK (1995), Vol. 4, p. 347.
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Comprehensive Organic Functional Group Transformations
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Gabbutt, C.D.1
Hepworth, J.D.2
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15
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0009206814
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note
-
5,12 of phosphites to thiocarbonyl groups have been proposed.
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-
-
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17
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0001591211
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S. Yoneda, T. Kawase, and Z. Yoshida, J. Org. Chem., 43, 1980 (1978); T. Kawase, S. Yoneda, and Z. Yoshida, Bull. Chem. Soc. Jpn., 52, 3342 (1979).
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J. Org. Chem.
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Yoneda, S.1
Kawase, T.2
Yoshida, Z.3
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18
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0001591211
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S. Yoneda, T. Kawase, and Z. Yoshida, J. Org. Chem., 43, 1980 (1978); T. Kawase, S. Yoneda, and Z. Yoshida, Bull. Chem. Soc. Jpn., 52, 3342 (1979).
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Bull. Chem. Soc. Jpn.
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Kawase, T.1
Yoneda, S.2
Yoshida, Z.3
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20
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0009197676
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note
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11
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21
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0009266326
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note
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2 to the ester 1c cannnot be excluded at the present stage.
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