“…Perhaps the most satisfactory technique, however, for utilizing the oxidizing capacity of hydrogen peroxide efficiently in organic reactions is to convert the active oxygen to the peracid form. Organic peracids can be readily prepared, usually with little loss of oxygen, by treating organic acids, acyl halides, or acid anhydrides with 25-100 per cent hydrogen peroxide or with inorganic peroxides (21,22,33,91,97,122,123,172,181,182,183,184,185,186,188,189,205,211,212,215,216,217,233,236,239,240,241,242,271,301,360,362,398,448,449,450,452,486,495,525). In many cases the peracid need not be isolated; it is sufficient to dissolve the substance to be oxidized in the organic acid or anhydride and add the hydrogen peroxide (4a, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, 20, 24, 35, 45a, 46, 405,406,412, 418, 421, 422, 423, 424, 434, 443, 457, 460, 461, 463, 477a, 483, 489, 490, 491, 492, 505, 506, 509, 524, 525, 537, 538, 541, 551, 552, 557).…”