The magnesiated uracil derivative can react with electrophiles to undergo substitution reactions. For example, reaction with alkyl halides can lead to the introduction of alkyl groups at specific positions on uracil.
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5-Pyrimidinecarbonitrile, 1,2,3,4-tetrahydro-2,4-dioxo-1,3-bis(phenylmethyl)-
3-Amino-2-(3,4-dimethoxy-phenyl)-propionic acid; hydrochloride
1H-Indene-2-thiol, 2,3-dihydro-1,1,3,3-tetramethyl-2-(phenylmethyl)-
1-Ethyl-2-(ethylthio)benzene
2(1H)-Quinolinone, 6,7-dichloro-4-hydroxy-3-phenyl-
2-(4-Methyl-benzoyl)-7-phenyl-thieno[2,3-b]pyridin-7-ium; bromide
E-1,2-bismethylsulphonyl-1-phenylpropene
2-methoxy-3-(pivaloylaminomethyl)benzoic acid
1-{4-nitrophenyl}-3,5-diphenyl-4,5-dihydro-1H-pyrazole
1,3,4-Thiadiazole-2(3H)-thione, 3-(hydroxymethyl)-5-phenyl-
2-nitro-1-(2,3,5,6-tetrafluorophenylthio)-1,3,4,4-tetrachloro-1,3-butadiene
C8H4F7NO3S2
Benzene, [[1-(ethylsulfonyl)ethyl]sulfonyl]-
ethyl pentafluorophenyl sulphide
THIENO[3,2-B]THIOPHENE-2-CARBOXYLIC ACID
Benzenecarboximidamide, 4-(octyloxy)-
5,6-dihydro-3-phenyl-4H-benzopyrrolo<2,1,5-cd>indolizin-4-one
CATECHIN-(4ALPHA->8)-EPICATECHIN
3-benzoyl-1-methoxycarbonylindolizine-5-carbaldehyde
4-((2-hydroxyphenyl)thio)benzonitrile
2-(trimethylsilylethynyl)-(2-propenyloxy)benzene
N4-(4-methylphenyl)-3,4-Pyridinediamine
methyl (4-acetyl-3-hydroxy-2-(methoxycarbonyl)-5-methyl)phenylacetate
2,3-bis(phenylthio)furo[3,2-b]pyridine
{C6H5CNSNS}(1+)*AsF6(1-)={C6H5CNSNS}{AsF6}
