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Updated: Jul 17, 2025

A Facile and Efficient Approach for the Production of Reversible Disulfide Cross-linked Micelles
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A Facile and Efficient Approach for the Production of Reversible Disulfide Cross-linked Micelles

Published on: December 23, 2016

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硫基化-甲基体型显示增强的脱效率和释放H2S

Lucie Wohlrábová1, Jana Okoročenkova2,3, Eduardo Palao2,3

  • 1Institute of Organic Chemistry and Biochemistry of the CAS, Flemingovo nám. 542/2, 160 00 Praha 6, Czech Republic.

Organic letters
|September 5, 2023
PubMed
概括

这项研究引入了一种新的硫酸的BODIPY光,实现了十倍更高的解效率. 这一突破使得硫化 (H2S) 的有效,可控释放用于生物研究.

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Design, Synthesis, and Photochemical Properties of Clickable Caged Compounds

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相关概念视频

Preparation and Reactions of Sulfides02:26

Preparation and Reactions of Sulfides

Sulfides are the sulfur analog of ethers, just as thiols are the sulfur analog of alcohol. Like ethers, sulfides also consist of two hydrocarbon groups bonded to the central sulfur atom. Depending upon the type of groups present, sulfides can be symmetrical or asymmetrical. Symmetrical sulfides can be prepared via an SN2 reaction between 2 equivalents of an alkyl halide and one equivalent of sodium sulfide.
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Electrophilic Aromatic Substitution: Sulfonation of Benzene01:22

Electrophilic Aromatic Substitution: Sulfonation of Benzene

Sulfonation of benzene is a reaction wherein benzene is treated with fuming sulfuric acid at room temperature to produce benzenesulfonic acid. Fuming sulfuric acid is a mixture of sulfur trioxide and concentrated sulfuric acid.
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Preparation and Reactions of Thiols02:33

Preparation and Reactions of Thiols

Thiols are prepared using the hydrosulfide anion as a nucleophile in a nucleophilic substitution reaction with alkyl halides. For instance, bromobutane reacts with sodium hydrosulfide to give butanethiol.
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