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
Your session will timeout in 10 minutes. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page. minute. You will be redirected to the HOME page after session timeout. Please click the button to continue session from the same page.