Iodine-Catalyzed Selective Synthesis of 2-Sulfanylphenols via Oxidative Aromatization of Cyclohexanones and Disulfides

Iodine‐catalyzed intermolecular dehydrogenative aromatizations of six‐membered cyclohexanones for the selective synthesis of 2‐sulfanylphenols have been developed. Both aryl and alkyl disulfides can be used as sulfanylation reagents to give the desired products in good yields under the optimized rea...

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Veröffentlicht in:Advanced synthesis & catalysis 2013-10, Vol.355 (14-15), p.3014-3021
Hauptverfasser: Ge, Wenlei, Zhu, Xun, Wei, Yunyang
Format: Artikel
Sprache:eng
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Zusammenfassung:Iodine‐catalyzed intermolecular dehydrogenative aromatizations of six‐membered cyclohexanones for the selective synthesis of 2‐sulfanylphenols have been developed. Both aryl and alkyl disulfides can be used as sulfanylation reagents to give the desired products in good yields under the optimized reaction conditions. The catalytic reaction uses dimethyl sulfoxide or oxygen as the terminal oxidant and avoids the use of transition metal catalysts. In addition, α‐sulfanyl enones could also be obtained via an iodine‐catalyzed oxidative system from simple cyclic ketones using dimethyl sulfoxide as the oxidant.
ISSN:1615-4150
1615-4169
DOI:10.1002/adsc.201300493