This implies that the reaction does not require the use of transition metals as catalysts. Many traditional cross-coupling reactions involve the use of transition metals, but the term "metal-free" suggests that this reaction achieves similar results without them.
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1-(2,4-dimethoxyphenyl)-2,2-bis(1-methyl-1H-indol-3-yl)ethanone
1-methyl-4-[(2-nitroethyl)sulfanyl]benzene
2,6-dimethyl-3,5-dimethoxycarbonyl-4-(2,4-dimethylphenyl)-1,4-dihydropyridine
(E)-2-(4-Chlorostyryl)quinoline
2H-Benzimidazol-2-one, 1,3-dihydro-1-(1-phenylethenyl)-
diethyl 2,2'-disulfanediylbis(4-(4-chlorophenyl)-6-methylpyrimidine-5-carboxylate)
3-(trifluoromethyl)-2-(4-(trifluoromethyl)phenyl)imidazo[1,2-a]pyridine
CHLORBENSIDE
Benzenesulfonamide, 4-chloro-N-(2-oxo-2-phenylethyl)-
1-DIPHENYLMETHYL-4-NITROSOPIPERAZINE
3-benzyl-1,4-dimethyl-1H-imidazol-2(3H)-one
(2-fluoro-2-(phenylsulfonyl)ethyl)benzene
2-(diphenylphosphoryl)-1-(naphthalen-2-yl)ethan-1-one
1,2-bis(3-fluorophenyl)-1,2-ethanediol
C14H12ClF3O5S
6-Methoxy-4-phenyl-2H-1-benzopyran-2-one
2-Propyn-1-one, 1-(3-chlorophenyl)-3-phenyl-
1-(3-(trifluoromethyl)phenyl)-3-(2,2-dimethylpent-4-enyl)urea
1-(hex-5-en-1-yloxy)-4-nitrobenzene
2-(2-methoxyphenyl)naphtho[1,2-d][1,3]oxazole
5-methoxy-2-(p-methoxyphenyl)benzoxazole
4-methylphenyl p-toluenesulfinate
1,3,5-tris(3-thiopheneyl)benzene
1-(tert-butyl)-4-(1-fluoroethyl)benzene
1-(4-bromophenyl)-2,4,5-triphenyl-1H-imidazole
Formamide, N-[(1R)-1-phenylethyl]-
