향기할로겐화물
반응은 일반적으로 방향 고리(방기)와 방향 고리에 연결된 할로겐 원자(대개 브로마이드 또는 요오드)가 들어 있는 유기 화합물인 두 개의 서로 다른 방향기 할로겐화물로 시작합니다.이 향기할로겐화물은 시작 원료로 사용된다.
화학 원료를 구입해야하는 경우 요청 정보를 제출하여최신견적을받으십시오.
향기할로겐화물의 학술 논문
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C - S coupling using
amixed-ligand Pd catalyst:Ahighly effective strategy for synthesizing arylthio-substituted heterocycles화학 물질
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2-(4-methoxyphenylthio)thiazole
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Synthesis of (arylalkenyl)silanes by palladium-catalyzed regiospecific and stereoselective allyl transfer from silyl-substituted homoallyl alcohols to aryl halides
화학 물질
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dimethyl(phenyl)-1-(1-phenylbutyl)silane
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Synthesis of amides via copper-catalyzed amidation of aryl halides using isocyanides
화학 물질
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4-acetyl-N-(2,4,4-trimethylpentan-2-yl)benzamide
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Palladium-catalyzed decarboxylative coupling of quinolinone-3-carboxylic acids and related heterocyclic carboxylic acids with (Hetero)aryl halides
화학 물질
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3-(4-fluorophenyl)-1-phenylquinolin-4(1H)-one
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SYNTHESIS OF ENOL ESTERS AND ENOL LACTONES VIA PALLADIUM-CATALYZED CARBONYLATION OF ARYL AND ALKENYL HALIDES
화학 물질
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Benzoic acid 1H-inden-2-yl ester
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Palladium-Catalyzed Double and Single Carbonylation of Aryl Halides and Allylic Compounds
화학 물질
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2-Propen-1-amine, N,N-diethyl-2-methyl-
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Biphenyl sulfonic acid ligands for catalytic C-N cross coupling of aryl halides with anilines and secondary amines
화학 물질
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4-Piperazinobenzonitrile
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Biphenyl sulfonic acid ligands for catalytic C-N cross coupling of aryl halides with anilines and secondary amines
화학 물질
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4-Piperazinobenzonitrile
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Palladium-Catalyzed Aminocarbonylation of Aryl Halides with N,N-Dialkylformamide Acetals
화학 물질
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N, N- 디메틸 -4- (트리 플루오로 메틸) 벤즈 아미드
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Ti/Ni-mediated inter- and intramolecular conjugate addition of aryl and alkenyl halides and triflates
화학 물질
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(3-acetylamino-phenyl)acetic acid methyl ester
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Nano copper oxide catalyzed synthesis of symmetrical diaryl selenides via cascade reaction of KSeCN with aryl halides
화학 물질
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bis(4-(benzyloxy)phenyl)selane
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Ni(II)/Zn catalyzed reductive coupling of aryl halides with diphenylphosphine oxide in water
화학 물질
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(Sp)-(-)-menthyl (4-methylphenyl)phenylphosphinate
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Palladium-catalysed Coupling of Trialkylstannyltetrathiafulvalenes with Aryl Halides
화학 물질
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Benzonitrile, 4-[2-(1,3-dithiol-2-ylidene)-1,3-dithiol-4-yl]-
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A practical palladium catalyzed dehalogenation of aryl halides and α-haloketones
화학 물질
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3-Benzylisoferulic acid methyl ester
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Palladium-catalyzed direct hydroxymethylation of aryl halides and triflates with potassium acetoxymethyltrifluoroborate
화학 물질
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(2- 메틸 벤조 [d] 옥사 졸 -5- 일) 메탄올
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New ligands for copper-catalyzed C-N coupling reactions with aryl halides
화학 물질
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1-(4-ethoxycarbonylphenyl)indole
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Stilbene synthesis through decarboxylative cross-coupling of substituted cinnamic acids with aryl halides
화학 물질
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3'-hydroxy-4''-methoxy-1,1-diphenylethene
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A versatile approach to 2,3-disubstituted indoles through the palladium-catalysed cyclization of oalkynyltrifluoroacetanilides with vinyl triflates and aryl halides
화학 물질
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1H-Indole, 2-butyl-3-(3,3,5,5-tetramethyl-1-cyclohexen-1-yl)-
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Aconvenient and efficient procedure for the palladium-catalyzed cyanation of aryl halides using trimethylsilylcyanide화학 물질
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trans-bromo[4-(trifluoromethyl)phenyl]bis(triphenylphosphine)palladium(II)
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Functionalized AB-type monomers for Suzuki polycondensation
화학 물질
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Benzenemethanol, 4-hexyl-
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Efficient recyclable CuI-nanoparticle-catalyzed S-arylation of thiols with aryl halides on water under mild conditions
화학 물질
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dodecyl 2-methylphenyl sulfide
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Synthesis of tetrasubstituted cyclopentadienes via palladium-catalyzed reaction of (Z)-2-En-4-yn acetates and N-methyl indoles
화학 물질
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1-methyl-3-(2,4,5-triphenyl-cyclopenta-1,4-dienyl)-1H-indole
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Attempts on N-amination of alkaloids
화학 물질
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3',4',5',6'-Tetrahydro-4',5'-dimethyl-6'-phenylspiro
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Picolinamide modified β-cyclodextrin/Pd (II) complex: Asupramolecular catalyst for Suzuki-Miyaura coupling of aryl, benzyl and allyl halides with arylboronic acids in water
화학 물질
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Benzene, 1-fluoro-4-(3-phenyl-2-propenyl)-
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C–C bond-forming reactions of ground-state aryl halides under reductive activation
화학 물질
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1-(2-((2-iodobenzyl) (methyl)amino)phenyl)-ethan-1-one
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