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Oxidation of Weakly Activated CH Bonds
Author(s) -
Reiser Oliver
Publication year - 1994
Publication title -
angewandte chemie international edition in english
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.831
H-Index - 550
eISSN - 1521-3773
pISSN - 0570-0833
DOI - 10.1002/anie.199400691
Subject(s) - reagent , yield (engineering) , surface modification , chemistry , selectivity , combinatorial chemistry , medicinal chemistry , organic chemistry , stereochemistry , materials science , catalysis , metallurgy
The functionalization of hydrocarbons by selective oxidation is of great technical importance. Two new, effective reagents, (perfluoroalkyl)oxaziridines 1a, b , hydroxylate the CH bonds at tertiary C atoms with high selectivity and in good yield. It remains to be seen if they are more economical and efficient than the tried‐and‐true dioxiranes and RuCl 3 /NaIO 4 .

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