Sulfonamides are a functional group that can act as a strong hydrogen bond donor. They are often used in asymmetric catalysis to facilitate the formation of key interactions between the catalyst and the substrate, thereby controlling the stereochemistry of the reaction.
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C26H28FN3O3S
2-Pentenoic acid, 5-[1-(triphenylmethyl)-1H-imidazol-4-yl]-, ethyl ester
4-CHLOROSULFONYL-BENZOIC ACID ETHYL ESTER
N-cyclohexylmethanesulfonamide
2-Pyrimidinamine, N-[(4-chlorophenyl)methyl]-
2-(cyclohex-2-en-1-yl)ethane-1-sulfonyl chloride
Ethanesulfonamide, N-(phenylmethyl)-2-(trimethylsilyl)-
1-benzoyl-1,2,3,4,5,6-hexahydro-4-phenyl<1,3,6>triazocino<1,2-a>benzimidazole
N-methyl-N-phenylpyridine-2-sulfonamide
N,N-diethyl-4-cyanobenzenesulfonamide
Benzenesulfonamide, N-[1,2,3,3a,4,8b-hexahydro-3a-hydroxy-6,8b-dimethyl-1-oxo-4-(phenyl methyl)cyclopent[b]indol-7-yl]-4-methyl-N-(phenylmethyl)-
4-(4-Chlorophenylsulfonyl)Morpholine, 97%
4-nitro-N-(3-phenylpropyl)benzamide
