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Volumn 47, Issue 34, 2006, Pages 6011-6016

Practical Cu-catalyzed amination of functionalized heteroaryl halides

Author keywords

[No Author keywords available]

Indexed keywords

COPPER; FUNCTIONAL GROUP; HALIDE; MORPHOLINE; NICOTINAMIDE DERIVATIVE;

EID: 33746211248     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.06.119     Document Type: Article
Times cited : (28)

References (22)
  • 1
    • 12344337315 scopus 로고    scopus 로고
    • For reviews of Pd catalyzed reaction, see:
    • For reviews of Pd catalyzed reaction, see:. Schlummer B., and Scholz U. Adv. Synth. Catal. 346 (2004) 1599
    • (2004) Adv. Synth. Catal. , vol.346 , pp. 1599
    • Schlummer, B.1    Scholz, U.2
  • 3
    • 0345708168 scopus 로고    scopus 로고
    • For reviews of Cu catalyzed reactions, see
    • For reviews of Cu catalyzed reactions, see. Ley S.V., and Thomas A.W. Angew. Chem., Int. Ed. 42 (2003) 5400
    • (2003) Angew. Chem., Int. Ed. , vol.42 , pp. 5400
    • Ley, S.V.1    Thomas, A.W.2
  • 6
    • 0003607021 scopus 로고    scopus 로고
    • For a general review of heterocycles see:. Katritzky A.R., and Rees C.W. (Eds), Elsevier, Oxford
    • For a general review of heterocycles see:. In: Katritzky A.R., and Rees C.W. (Eds). Comprehensive Heterocyclic Chemistry II (1996), Elsevier, Oxford
    • (1996) Comprehensive Heterocyclic Chemistry II
  • 20
    • 33746186589 scopus 로고    scopus 로고
    • note
    • All microwave reactions were performed using a Personal Chemistry Emrys™ Optimizer in a septa capped 0.50-2 mL Biotage™ microwave vial with magnetic stirring. Power required to maintain target temperature was controlled by Emrys™ Optimizer Software.
  • 21
    • 33746247426 scopus 로고    scopus 로고
    • note
    • Samples were purified by preparative HPLC on a Waters Nova-Pak HR C18 6 μm 60 Å Prep-Pak cartridge column (40 mm × 100 mm). A gradient of acetonitrile (A) and 0.1% trifluoroacetic acid in water (B) was used, at a flow rate of 70 mL/min (0-0.5 min 10% A, 0.5-12.0 min linear gradient 10-95% A, 12.0-15.0 min 95% A, 15.0-17.0 min linear gradient 95-10% A). Samples were injected in 2.5 mL of DMSO/MeOH (1:1).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.