Selectivity of aromatic chlorination reactions within a reversed-phase liquid chromatography column
Substrate selelctivity, coupled with modest regioselectivity, was obtained in the monochlorination of a series of -alkyl phenyl ethers by chlorine water on a reversed-phase high performance liquid chromatography column.
References (13)
- et al.
Anal. Chem.
(1985)et al.J. Am. Chem. Soc.
(1984)et al.J. Phys. Chem.
(1983)et al.J. Liq. Chromatogr.
(1983) J. Am. Chem. Soc.
(1933)- et al.
J. Chromatogr.
(1977) - et al.
J. Am. Chem. Soc.
(1957)et al.
There are more references available in the full text version of this article.
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