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Synlett

Volumn , Issue 12, 2007, Pages 1836-1842

A mild and efficient method for copper-catalyzed Ullmann-type N-arylation of aliphatic amines and amino acids

(5) Jiang, Qun a Jiang, Deshou b Jiang, Yuyang a Fu, Hua b Zhao, Yufen b

a TSINGHUA UNIVERSITY (China)

b Tsinghua University (China)

Author keywords

Aliphatic amine; Amino acid; Copper catalyzed; Ullmann reaction

Indexed keywords

2 (4 CHLOROPHENYLAMINO) 4 METHYLPENTANOIC ACID; 3 BENZYL 3,4 DIHYDROXYQUINOXALIN 2(1H) ONE; 3,4 DIHYDROQUINOXALIN 2(1H) ONE DERIVATIVE; AMINE; AMINO ACID; COPPER; DIHYDROXYQUINOLIN 2(1H) ONE DERIVATIVE; KETONE DERIVATIVE; N BENZYL 4 METHYLBENZENAMINE; TIN CHLORIDE; UNCLASSIFIED DRUG;

ARTICLE; ARYLATION; CATALYSIS; CHEMICAL REACTION; CHEMICAL STRUCTURE;

EID: 34547621822 PISSN: 09365214 EISSN: None Source Type: Journal
DOI: 10.1055/s-2007-982564 Document Type: Article

Times cited : (74)

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- Synthesis of Ligands Ligands L1-L4 were prepared according to the reported procedures. 18,19 General Procedure A: Coupling of Aryl Iodides with Amines: A flask was charged with CuI (19 mg, 0.1 mmol, ligand (0.2 mmol, K3PO4 (424 mg, 2 mmol, and any remaining solid (amine and/or aryl halide, The flask was evacuated and backfilled with nitrogen. Aryl iodide (1 mmol, if liquid) and amine (1.5 mmol, if liquid, and DMF (1.0-1.5 mL) were added to the flask under a nitrogen atmosphere. The mixture was allowed to stir under the nitrogen atmosphere at the shown temperature for the indicated period of time see Table 2, After completion of the reaction, the mixture was diluted with EtOAc, the solution was filtered, and the inorganic salts were removed. The solvent in the filtrate was removed with the aid of a rotary evaporator, and the residue was purified by column chromatography on silica gel
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.