One‐pot synthesis of 2‐aminobenzothiazoles using a new reagent of [bmim]br<sub>3</sub>in [bmim]BF<sub>4</sub>
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<jats:title>Abstract</jats:title><jats:p><jats:chem-struct-wrap><jats:chem-struct><jats:graphic xmlns:xlink="http://www.w3.org/1999/xlink" mimetype="image/gif" position="anchor" specific-use="enlarged-web-image" xlink:href="graphic/must001.gif"><jats:alt-text>magnified image</jats:alt-text></jats:graphic></jats:chem-struct></jats:chem-struct-wrap></jats:p><jats:p>The one‐pot direct synthesis of 2‐aminobenzothiazoles from phenyl isothiocyanate and amines using a new reagent of 1‐butyl‐3‐methylimidazolium tribromide ([Bmim]Br<jats:sub>3</jats:sub>) in ionic liquid 1‐butyl‐3‐methylimidazolium tetraflouoroborate ([Bmim]BF<jats:sub>4</jats:sub>) is described.</jats:p>
収録刊行物
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- Journal of Heterocyclic Chemistry
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Journal of Heterocyclic Chemistry 43 (4), 1123-1124, 2006-07
Wiley