Published TCIMAIL newest issue No.198
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Novel Selective Iodinating Reagent
N,N-Dimethyl-N-(methylsulfanylmethylene)ammonium
iodide developed by Porter et al. is a novel selective iodinating reagent, which can convert primary
and secondary alcohols to the corresponding iodo compounds. In particular, primary alcohols react more rapidly
than secondary alcohols, which allows selective iodination of primary hydroxy groups or in primary-secondary
diols.
References
- Selective Conversion of Alcohols into Alkyl Iodides Using a Thioiminium Salt