1,2-Ethanedisulfenyl chloride as a reagent for the preparation of ethylenedithio substituted aromatics.

doi:10.1016/S0379-6779(00)01227-3

Paper

1,2-Ethanedisulfenyl chloride as a reagent for the preparation of ethylenedithio substituted aromatics.

Published Mar 15, 2001 · Fredrik Allared, Jan Blid, J. Hellberg

Synthetic Metals

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6

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0

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Abstract

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Study Snapshot

1,2-ethanedisulfenyl chloride is a promising reagent for the preparation of dihydro-1,4-dithiino substituted aromatics in modest yields.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

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Paper

1,2-Ethanedisulfenyl chloride as a reagent for the preparation of ethylenedithio substituted aromatics.

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References

Citations

3,4-Dithiaphosphole and 3,3',4,4'-tetrathia-1,1'-biphosphole π-conjugated systems: S makes the impact.

S atoms in phosphole-based conjugated systems decrease HOMO-LUMO separation and stabilize the LUMO level, impacting their electronic properties and potential applications in polymerization.

Persulfurated aromatic compounds.

Persulfurated aromatic compounds offer unique properties and potential for designing redox sensors, ion-selective membranes, and nonlinear optical materials.

1,4-Dioxins, Oxathiins, Dithiins, and their Benzo Derivatives

This chapter updates the literature on 1,4-dioxins, oxathiins, dithiins, and their benzo derivatives, focusing on their reactivity, synthesis, and applications in organic and medicinal chemistry.

Recent progress in the chemistry of sulfur-containing indoles

Recent progress in the chemistry of sulfur-containing indoles has led to the development of interesting compounds with potent biological activity profiles.