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Volumn 62, Issue 16, 1997, Pages 5526-5536

Novel ipso-Substitution of p-Sulfinylphenols through the Pummerer-Type Reaction: A Selective and Efficient Synthesis of p-Quinones and Protected p-Dihydroquinones

Author keywords

[No Author keywords available]

Indexed keywords

HYDROQUINONE DERIVATIVE; PHENOL DERIVATIVE; STYRENE;

EID: 0030843120     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo970418o     Document Type: Article
Times cited : (34)

References (69)
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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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    • 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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    • 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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