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2000
The article contains sections titled: 1. Sulfones 1.1. Physical and Chemical Properties 1.2. Synthesis 1.2.1. Oxidation of Thioethers (Sulfides) 1.2.2. Alkylation of Sulfinic Acid Derivatives 1.2.3. Addition of Sulfinic Acid Derivatives to Multiple Bonds 1.2.4. Rearrangement of Sulfinates 1.2.5. Sulfones from Sulfonyl Carbanions 1.2.
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The article contains sections titled: 1. Sulfones 1.1. Physical and Chemical Properties 1.2. Synthesis 1.2.1. Oxidation of Thioethers (Sulfides) 1.2.2. Alkylation of Sulfinic Acid Derivatives 1.2.3. Addition of Sulfinic Acid Derivatives to Multiple Bonds 1.2.4. Rearrangement of Sulfinates 1.2.5. Sulfones from Sulfonyl Carbanions 1.2.
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Angewandte Chemie International Edition in English, 1972
Hans Bock, Bahman Solouki
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Hans Bock, Bahman Solouki
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Journal of the American Veterinary Medical Association, 1984
E M, Alsup, R M, DeBowes
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E M, Alsup, R M, DeBowes
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1977
Sulfoxides are formed by partial oxidation of sulfides, which upon further oxidation are converted to sulfones, and hence may be considered as a very stable intermediate in the oxidation process. However, since the sulfur-oxygen linkage in sulfoxides is polarized and much weaker than that in sulfones, sulfoxides are relatively reactive and undergo many
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Sulfoxides are formed by partial oxidation of sulfides, which upon further oxidation are converted to sulfones, and hence may be considered as a very stable intermediate in the oxidation process. However, since the sulfur-oxygen linkage in sulfoxides is polarized and much weaker than that in sulfones, sulfoxides are relatively reactive and undergo many
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Gas-phase photolysis of sulfoxides. Tetramethylene sulfoxide
The Journal of Physical Chemistry, 1980K. E. Salomon, F. H. Dorer
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