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Sulfones and Sulfoxides

Authors: Kathrin‐Maria Roy;

Sulfones and Sulfoxides

Abstract

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 1.2.6. Addition of Sulfur Dioxide 1.3. Reactions 1.4. Industrial Uses 2. Sulfoxides 2.1. Physical and Chemical Properties 2.2. Synthesis 2.2.1. Oxidation of Sulfides 2.2.2. Reaction of Sulfur Dioxide with Aromatics 2.2.3. Sulfoxides from Sulfinates 2.2.4. α,β-Unsaturated Sulfoxides 2.2.5. Optically Active Sulfoxides 2.3. Reactions 2.3.1. Reactions of α-Sulfinyl Carbanions 2.3.2. Reactions with Grignard Reagents 2.3.3. Pummerer Rearrangement 2.3.4. Oxidation and Reduction 2.4. Uses 2.5. Dimethyl Sulfoxide 2.5.1. Production 2.5.2. Uses 2.5.3. Reactions 3. Toxicology 3.1. Sulfones 3.2. Dimethyl Sulfoxide 4. Acknowledgement

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
16
Top 10%
Top 10%
Average
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