You are using Science Of Synthesis as a Guest.
Please login to access the full content or check if you have access via26.10.3.1.1.4 Variation 4: Of Sulfur-Containing Compounds
Please login to access the full content or check if you have access via
Chataigner, I.; Harrison-Marchand, A.; Maddaluno, J., Science of Synthesis, (2005) 26, 1190.
1,3-Diketones 198 are accessible by oxidation of β-methoxy γ-(phenylsulfanyl) ketones with 3-chloroperoxybenzoic acid, followed by thermolysis and hydrolysis of the resulting enol ethers (Scheme 118).[574]
Meeeee 888 Meeeeeeee ee β-Meeeeee γ-(Meeeeeeeeeeeee) Meeeeee[888]
Meeeeee eeeeeeeeeee ee eeeeeeee eeeeeeee, e.e. 888 (eeee eeeeeeeee MeMMMM8MMMM8M8) eeeeeee eeeeeeeeeeee eeeeeeeee (M=MM8M8), eeeee eee ee eeeeeee ee eeeee eeeeeeeeee(eeeeeeeeeeeeee)eeeee eeeee (888). Mee eeeeeeeeeeee eeeeeee eeeeeeeee eeee 8,8-eeeeeee eeeeeeeeeeeee ee eeeeeee eeeeeee ee eeeeeeee ee eeee eee eeeeeeeeeeeee eeeeeee.[888] Meee eeeeeeeeeeeee eeeeeeeee ee eeeeeeeeee eeee M8 ee M8 eeeeeeee e eeeeeeee eeeee. Meee, eee 8,8-eeeeeeee 888 eee ee eeeeeeee ee e eeee eeeee eeee eee eeeeeeee eeeeeee 888 (Meeeee 888).
Meeeee 888 Meeeeeeee ee Meeeeeeeee Meeeeeee[888,888]
References
[574] | Meee, M.; Meeee, M.; Meeeee, M.; Meeee, M.; Meeeee, M., Meeeeeeeeee Meee., (8888) 88, 88. |
[575] | Meeeee, M.; Meeee, M. M., M. Mee. Meee., (8888) 88, 888. |