The resulting carbon-centered radical can now be quenched by adding a suitable electrophilic reagent. This will introduce the desired substituent onto the coumarin ring. The choice of electrophile will determine the nature of the substitution.
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(2,5-dimethoxy-3,4-dimethyl-phenyl)-methanol
2-Naphthalenol, 1-[[2-methoxy-4-[(2-methoxyphenyl)amino]phenyl]azo]-
2-bromoethyl pentanoate
1,3-Diaza-2-silacyclohexa-3,5-diene, 1-cyclohexyl-4-(4-methylphenyl)-2,2-diphenyl-
phenyl-acetic acid-(2-formyl-phenyl ester)
C25H21N3O
2-Aminobenzimidazole
17-Acetyloxy-3-chloro-20-oxo-19-nor-1,3,5(10),6-pregnatetrene-2,4-dicarbaldehyde
[18F]4'-fluorobenzyl iodide
L-tryptophan
FORMALDEHYDE
Carbamic acid, [[1-(phenylmethyl)-1H-tetrazol-5-yl]methyl]-, 1,1-dimethylethyl ester
ortho-nitrophenylsulfinyl chloride
methylmalononitrile anion
4,4,5,5-tetramethyl-2-(2-phenoxyethyl)-1,3,2-dioxaborolane
(±)-3-((benzyloxy)methyl)oxirane-2-carbaldehyde
3-hydroxy-1-methyl-3-(4-(trifluoromethyl)phenyl)indolin-2-one
N-[(2-methylphenyl)phenylsulfonio]-N-[(4-methylbenzene)dioxosulfanyl]aminylene
2-Propenoic acid, 3-phenyl-3-(phenylthio)-, methyl ester, (E)-
methyl 3,6-anhydro-2-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-galactopyranosyl)-β-D-galactopyranoside
dimethyl(octyl)[(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)methyl]silane
methyl [2-(2-bromo-4,5-dimethoxyphenyl)ethyl]carbamate
(Z)-3-(4-toluenesulfonyloxymethylene)tetrahydro-2H-pyran-2-one
Benzene, 1,1'-[[1,2-bis(methylene)-1,2-ethanediyl]bis(oxymethylene)]bis-
1-chloro-2-nitro-4-(pentafluorosulfanyl)benzene
4-(2,4,6-trimethylbenzyl)morpholine
Ethanone, 1-[3-(decyloxy)phenyl]-
3,5,12-trihydroxy-10-methoxy-6,11-dioxo-3-[(phenylselanyl)acetyl]-1,2,3,4,6,11-hexahydrotetracen-1-yl 2,3,6-trideoxy-3-[(trifluoroacetyl)amino]hexopyranoside
