술파민
술파민계 화합물은 강한 수소결합 공여체로 활용될 수 있는 관능단이다.이들은 촉매와 바닥물 사이의 키 상호작용의 형성을 촉진하여 반응의 입체화학을 제어하기 위해 비대칭 촉매에 자주 사용된다.
화학 원료를 구입해야하는 경우 요청 정보를 제출하여최신견적을받으십시오.
술파민의 학술 논문
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ω-(Imidazol-4-yl)alkane-1-sulfonamides: a new series of potent histamine H3 receptor antagonists
화학 물질
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2-Pentenoic acid, 5-[1-(triphenylmethyl)-1H-imidazol-4-yl]-, ethyl ester
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A convenient synthesis of N-alkyl-(E)-1-alkenesulfonamides
화학 물질
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N-cyclohexylmethanesulfonamide
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Facile one-pot synthesis of aromatic and heteroaromatic sulfonamides
화학 물질
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4- 클로로 포닐-벤조산 에틸 에스테르
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Manganese dioxide catalyzed N-alkylation of sulfonamides and amines with alcohols under air
화학 물질
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2-Pyrimidinamine, N-[(4-chlorophenyl)methyl]-
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Enantioselective Radical Construction of 5-Membered Cyclic Sulfonamides by Metalloradical C-H Amination
화학 물질
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2-(cyclohex-2-en-1-yl)ethane-1-sulfonyl chloride
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Efficient and Practical Synthesis of Sulfonamides Utilizing SO2 Gas Generated on Demand
화학 물질
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4- (4- 클로로 페닐 설 포닐) 모르 폴린, 97 %
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Inhibition of the α-carbonic anhydrase from Vibrio cholerae with amides and sulfonamides incorporating imidazole moieties
화학 물질
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4-nitro-N-(3-phenylpropyl)benzamide
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Copper-catalyzed N-alkylation of sulfonamides with benzylic alcohols: Catalysis and mechanistic studies
화학 물질
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Ethanesulfonamide, N-(phenylmethyl)-2-(trimethylsilyl)-
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Class III Antiarrhythmic Activity of Novel Substituted 4-<(Methylsulfonyl)amino>benzamides and Sulfonamides
화학 물질
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1-benzoyl-1,2,3,4,5,6-hexahydro-4-phenyl<1,3,6>triazocino<1,2-a>benzimidazole
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Synthesis of Heteroaryl Sulfonamides from Organozinc Reagents and 2,4,6-Trichlorophenyl Chlorosulfate
화학 물질
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N-methyl-N-phenylpyridine-2-sulfonamide
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I2/TBHP Mediated C-N and C-H Bond Cleavage of Tertiary Amines toward Selective Synthesis of Sulfonamides and β-Arylsulfonyl Enamines: The Solvent Effect on Reaction
화학 물질
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N,N-diethyl-4-cyanobenzenesulfonamide
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A facile removal of the arenesulfonyl group by electrochemical reduction of sulfonamides in a new cooperative system of anthracene and ascorbic acid: The control of crisscross annulation
화학 물질
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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)-
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