Facile Introduction of SH Group on Aromatic Substrates via Electrophilic Substitution Reactions

Simple item page
dc.contributor.authorJean-Michel Becht
dc.contributor.authorAlain Wagner
dc.contributor.authorCharles Mioskowski
dc.date.accessioned2012-11-15T06:18:07Z
dc.date.accessioned2025-02-17T14:01:23Z
dc.date.available2012-11-15T06:18:07Z
dc.date.issued2012-11-14
dc.descriptionHerein, we describe a mild and efficient two-step procedure to introduce a thiol group on aromatic substrates. First, reaction with an activated sulfoxide leads to an arylsulfonium salt intermediate. Then, two successive â- elimination-based dealkylation reactions afford the desired arylthiols in good to excellent yieldsen_US
dc.description.abstractHerein, we describe a mild and efficient two-step procedure to introduce a thiol group on aromatic substrates. First, reaction with an activated sulfoxide leads to an arylsulfonium salt intermediate. Then, two successive â- elimination-based dealkylation reactions afford the desired arylthiols in good to excellent yieldsen_US
dc.identifier.urihttps://dl.ftveti.edu.et/handle/123456789/4113
dc.language.isoenen_US
dc.subjectFacile Introduction of SH Group on Aromatic Substrates via Electrophilic Substitution Reactionsen_US
dc.titleFacile Introduction of SH Group on Aromatic Substrates via Electrophilic Substitution Reactionsen_US
dc.typeArticleen_US

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
505759 (65).pdf
Size:
81 KB
Format:
Adobe Portable Document Format
Download

Collections

FTVETI Collections