An efficient sulfenylation of aromatics using highly active quinone mono O , S -acetal bearing a pentafluorophenylthio group

Author:

Matsugi Masato,Murata Kenji,Nambu Hisanori,Kita Yasuyuki

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference8 articles.

1. .alpha.-Sulfenylated carbonyl compounds in organic synthesis

2. Organic Chemistry of Sulfur;Oae,1977

3. For examples: Ref. 1 and (a) Anzai, K. J. Heterocycl. Chem.1979, 16, 567–569. (b) Atkinson, J. G.; Hamel, P.; Girard, Y. Synthesis1988, 480–481. (c) Criatau, H. J.; Chabaud, B.; Chene, A.; Christol, H. Synthesis1981, 892–894. (d) Bottino, F.; Fradullo, R.; Pappalardo, S. J. Org. Chem.1981, 46, 2793–2795. (e) Oae, S.; Shinhana, K.; Kim, Y. H. Chem. Lett.1979, 939–942. (f) Bates, D. K.; Tafel, K. A. J. Org. Chem.1994, 59, 8076–8080. (g) Kita, Y.; Takada, T.; Mihara, S.; Whelen, B. A.; Tohma, H. J. Org. Chem.1995, 60, 7144–7148: this method is effective for the sulfenylation of aromatic compounds; but is not suitable for heteroaromatic compounds.

4. Isolation of the Quinone MonoO,S-Acetal Intermediates of the Aromatic Pummerer-Type Rearrangement ofp-Sulfinylphenols with 1-Ethoxyvinyl Esters

5. A novel efficient sulfenylation method using quinone mono-O,S-acetals under mild conditions

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