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The compound 13 and its decomposition product, PhSS (O)Ph, seem to be the plausible reductive species, although their reduction mechanisms have not been cleared yet. See: (a) Bell, P. A.; Hogg, D. R.; Robertson, A. J. Chem. Soc., Perkin Trans. 1 1978, 1246. (b) Block, E.; O'Connor, J. J. Am. Chem. Soc. 1974, 96, 3921. (c) Morishita, T.; Furukawa, N.; Oae, S. Tetrahedron 1981, 37, 3115.
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Hogg, D.R.2
Robertson, A.3
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65
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13044298399
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The compound 13 and its decomposition product, PhSS (O)Ph, seem to be the plausible reductive species, although their reduction mechanisms have not been cleared yet. See: (a) Bell, P. A.; Hogg, D. R.; Robertson, A. J. Chem. Soc., Perkin Trans. 1 1978, 1246. (b) Block, E.; O'Connor, J. J. Am. Chem. Soc. 1974, 96, 3921. (c) Morishita, T.; Furukawa, N.; Oae, S. Tetrahedron 1981, 37, 3115.
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Block, E.1
O'Connor, J.2
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0001134396
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The compound 13 and its decomposition product, PhSS (O)Ph, seem to be the plausible reductive species, although their reduction mechanisms have not been cleared yet. See: (a) Bell, P. A.; Hogg, D. R.; Robertson, A. J. Chem. Soc., Perkin Trans. 1 1978, 1246. (b) Block, E.; O'Connor, J. J. Am. Chem. Soc. 1974, 96, 3921. (c) Morishita, T.; Furukawa, N.; Oae, S. Tetrahedron 1981, 37, 3115.
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Oae, S.3
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Very recently, we have applied this transformation to a novel and efficient synthesis of peri-hydroxydihydroquinone derivatives. Kita, Y.; Takeda, Y.; Iio, K.; Yokogawa, K.; Takahashi, K.; Akai, S. Tetrahedron Lett. 1996, 37, 7545.
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Minisci, F.; Citterio, A.; Vismara, E.; Fontana, F.; De Bernardinis, S. De J. Org. Chem. 1989, 54, 728.
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