C-H functionalization is a powerful strategy in organic synthesis that involves the selective activation of C-H bonds in organic molecules and their conversion into other functional groups or bonds, such as C-C or C-N bonds.
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Diethyl 1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate
methyl 2-methyl-4-oxo-4H-chromene-3-carboxylate
5-(4-chloro-phenyl)-oxazole-2-carboxylic acid
(4S,5R,E)-methyl 5-(cyclopent-1-en-1-yl)-5-methoxy-4-(4-methoxyphenyl)pent-2-enoate
(2-amino-5-bromophenyl)(pyrrolidin-1-yl)methanone
Methanesulfonic acid 5-bromo-2-methyl-4-(1-methyl-2,5-dioxo-cyclopentylmethyl)-phenyl ester
C24H34O5Si
3-(4-chlorophenyl)-5,6-diphenyl-2H-pyran-2-one
1,2,3,4-tetrabutyl-6-isopropylnaphthalene
1,3-diphenyl-3-pyridin-2-ylamino-propenone
2-heptyl-1,4-dimethoxybenzene
N-(2-bromophenyl)-N-methylnitrous amide
2,3,5-triphenyl-1-(pyrimidin-2-yl)-1H-indole
4-methoxy-2,4'-dimethyldiphenyl thioether
bis(3-acetoxyphenyl)-2-pyridylmethane
3-phenyl-5-p-tolyl-4,5-dihydroisoxazol-5-ol
