Application of "click" chemistry in solid phase synthesis of alkyl halides

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Abstract

A convenient and highly selective microwave assisted procedure for the conversion of allylic, benzylic and aliphatic alcohols to their corresponding halides using polymer-bound triphenylphosphine and iodine is presented. In case of symmetrical diols, mono-iodination product is obtained in very high yield. Additionally, highly regioselective behavior is observed in our procedure. Simplicity in operation, no column chromatography required for the purification of the products, recyclability of the reagents used, short reaction times and good to excellent yields are the advantages of our protocol. Most functional groups remain unaffected under our reaction condition.

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Das, D., Chanda, T., & Rokhum, L. (2015). Application of “click” chemistry in solid phase synthesis of alkyl halides. Acta Chimica Slovenica, 62(4), 775–783. https://doi.org/10.17344/acsi.2015.1478

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