The reaction may terminate with the combination of two radicals to form a non-radical product. This step helps in preventing the accumulation of radicals and ensures the formation of the desired acylated compound.
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(4-bromophenyl)(pyrazin-2-yl)methanone
erythro-4-benzyloxy-5-methyl-3-(tetrahydro-2-pyranyloxy)-5-hexen-1-yne
(R)-1-((4S,6R)-6-(2-(benzyloxy)ethyl)-2,2-dimethyl-1,3-dioxan-4-yl)pent-4-en-2-ol
(+/-)-(3R,4S)-3-benzylchroman-4-ol
cis-2-benzyl-1-(4-nitro-phenyl)-1,2,3,4-tetrahydro-9H-β-carboline-3-carboxylic acid ethyl ester
(E)-4-[Benzenesulfonyl-(3-oxo-propyl)-amino]-but-2-enoic acid ethyl ester
(5R)-5-methyl-1-(2-propen-1-yl)-2-(2-propen-2-yl)cyclohexene
(+)-PULEGONE
Menthone
9-isopropylsulfane-9H-fluorene
C23H23NO3
METHANOL
C29H26F3O6PRuS2
diethyl (2-oxo-4-(p-methoxyphenyl)-2H-chromen-3-yl)phosphonate
Z-2-(4-chlorobut-2-enyl)cyclohexanone
Ether
Cyclohexanone
palladium acetate
ethyl (RS)-(all-E)-4-methylfarnesate
4-hydroxy-4-methyl-6-(2,6,6-trimethylcyclohex-1-en-1-yl)hex-2-ynyl acetate
ethyl 1,2-dihydro-6-methyl-2-oxo-4-(2-phenylethyl)pyrimidine-5-carboxylate
(4S,5R)-4-(2-hydroxypropan-2-yl)-5-((-)-menthyloxy)-dihydrofuran-2(3H)-one
Linoleic Acid
hydrogen peroxide
SODIUM BOROHYDRIDE
