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1 n reduction in the presence of a coreactant (benzoyl peroxide).
2 dimethylaniline encounter interfaces bearing benzoyl peroxide.
3 photochemical reaction between graphene and benzoyl peroxide.
5 ntaining benzene 85 wt%, ethanol 14 wt%, and benzoyl peroxide 1.0 wt%; but with each at 0.018 molal c
6 mine whether repeated topical treatment with benzoyl peroxide, a source of free radicals, produced th
8 -HO)(B(C6F5)3)2] 4 with isobutene while with benzoyl peroxide afforded [Cp*2Fe][PhC(O)OE(C6F5)3] (E =
11 excited graphene transfers a hot electron to benzoyl peroxide and induces its decomposition to a phen
12 0.16 to 0.50% was observed upon addition of benzoyl peroxide as a coreactant in the above electrolyt
16 region only to the reduction side and using benzoyl peroxide (BPO) as a coreactant, strong ECL of TA
18 oreactant such as tri-n-propylamine (TPA) or benzoyl peroxide (BPO), BB3 and BB4 exhibit strong ECL a
22 n with N-bromosuccinimide in the presence of benzoyl peroxide gave 2,4-bis(pivaloylamino)-6-bromo-5-(
23 6%) of 127 assigned topical erythromycin and benzoyl peroxide in a combined formulation plus oral pla
24 t secondary amines can be directly used with benzoyl peroxide in a one-pot procedure that proceeds vi
26 ntent, although the highest concentration of benzoyl peroxide increased epidermal thickness and glyco
27 rotected secondary amine sites, free radical benzoyl peroxide initiated polymerization, deprotection
28 vere acne, but only with a topical retinoid, benzoyl peroxide, or their combination, and ideally for
29 al placebo, 78 (60%) of 130 assigned topical benzoyl peroxide plus oral placebo, 84 (66%) of 127 assi
30 lts indicate that repeated administration of benzoyl peroxide produces skin changes in the hairless m
33 ycline 12.3% (0.4 to 24.2); erythromycin and benzoyl peroxide separately versus combined formulation
34 To limit resistance, it is recommended that benzoyl peroxide should always be added when long-term o
35 need oral antibiotics combined with topical benzoyl peroxide to decrease antibiotic-resistant organi
36 -response slope in the presence of 40 microM benzoyl peroxide to that of irradiated controls was 4.3
37 response slopes in the presence of 40 microM benzoyl peroxide to that of irradiated controls was 4.7
39 CI -13.3 to 10.9); combined erythromycin and benzoyl peroxide versus oxytetracycline 11.1% (-0.7 to 2
40 s combined formulation -3.5% (-15.2 to 8.2); benzoyl peroxide versus oxytetracycline 5.0% (-7.0 to 17
41 tial synergistic effect of ultraviolet B and benzoyl peroxide was below the level of detection used i
42 n 355 nm-irradiated cells in the presence of benzoyl peroxide was inhibited in a concentration-depend
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