N‑Chlorosuccinimide-Promoted Regioselective Sulfenylation of Imidazoheterocycles at Room Temperature

Regioselective sulfenylation of imidazoheterocycles with thiophenols at room temperature is reported. Sulfenylation is promoted by N-chlorosuccinimide under metal-free conditions with a broad range of substrate scopes.

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Bibliographic Details
Published inOrganic letters Vol. 16; no. 11; pp. 2978 - 2981
Main Authors Ravi, Chitrakar, Chandra Mohan, Darapaneni, Adimurthy, Subbarayappa
Format Journal Article
LanguageEnglish
Published WASHINGTON American Chemical Society 06.06.2014
Amer Chemical Soc
Subjects
ambient temperature
chemical reactions
chemical structure
Chemistry
Chemistry, Organic
organic compounds
Physical Sciences
regioselectivity
Science & Technology
FACILE SYNTHESIS
ONE-POT SYNTHESIS
CATALYZED C-S
COUPLING REACTION
ANTIVIRAL ACTIVITY
BOND FORMATION
DERIVATIVES
EFFICIENT
INDOLES
AMINOOXYGENATION
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Summary:Regioselective sulfenylation of imidazoheterocycles with thiophenols at room temperature is reported. Sulfenylation is promoted by N-chlorosuccinimide under metal-free conditions with a broad range of substrate scopes.
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ISSN:1523-7060
1523-7052
1523-7052
DOI:10.1021/ol501117z