59951-00-7Relevant articles and documents
Transformation of tertiary benzyl alcohols into the vicinal halo-substituted derivatives using N-Halosuccinimides
Ajvazi, Njomza,Stavber, Stojan
supporting information, (2016/11/02)
The efficiency of direct conversion of tertiary alcohols bearing a-hydrogen atom to vicinal halohydrins-chlorohydrins and bromohydrins-under green reaction conditions was tested preliminarily on modeltertiary benzyl alcohols. Tertiary alcohols were successfully directly halogenated to vicinal halohydrins with N-halosuccinimide in aqueous media. The efficiency of the reaction in water was significantly improved in the presence of sodium dodecyl sulphate as the surfactant.
(Dichloroiodo)benzene - An Easily Available Reagent for Chloro- and Iodoalkoxylation, Iodohydroxylation, and Iodochlorination of Alkenes
Yusubov,Yusubova,Filimonov,Chi, Ki-Whan
, p. 443 - 450 (2007/10/03)
A convenient synthesis of vicinal methoxychlorides, methoxyiodides, iodhydrines and iodochloride from alkenes using PhICl2/CH 3OH, I2/ PhICl2/CH3OH, I 2/PhICl2/CH3CN/H2O and I 2/PhICl2/CH2Cl2 is described.
Iodosobenzene dichloride, a convenient reagent for chloro- and iodomethoxylation of double and triple bonds
Yusubov,Yusubova,Filimonov,Ki-Whan, Chi
, p. 902 - 904 (2007/10/03)
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