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A New Facile Route to Chlorination of Alcohols via Lewis Acid AlCl<sub>3</sub>

A New Facile Route to Chlorination of Alcohols via Lewis Acid AlCl<sub>3</sub>
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摘要 Halogenated aluminates AlCl3, applied as efficient chlorination reagent for hydroxyl groups of substitution alcohols is described. Primary and secondary benzylic alcohols could be transformed into corresponding aromatic halides with almost complete conversion and unique selectivity. As chlorination reagent, AlCl3 has an incomparable advantage over others, such as low material cost, commercial availability as well as convenient product isolation. Halogenated aluminates AlCl3, applied as efficient chlorination reagent for hydroxyl groups of substitution alcohols is described. Primary and secondary benzylic alcohols could be transformed into corresponding aromatic halides with almost complete conversion and unique selectivity. As chlorination reagent, AlCl3 has an incomparable advantage over others, such as low material cost, commercial availability as well as convenient product isolation.
出处 《International Journal of Organic Chemistry》 2012年第1期21-25,共5页 有机化学国际期刊(英文)
关键词 ALCOHOLS Lewis Acid NUCLEOPHILES CHLORINATION Alcohols Lewis Acid Nucleophiles Chlorination
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