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Volumn 30, Issue 9, 2009, Pages 1931-1932

Ruthenium-catalyzed transfer hydrogenation of alkynes by tributylamine

Author keywords

Alkenes; Alkynes; Ruthenium catalyst; Transfer hydrogenation; Tributylamine

Indexed keywords


EID: 75649137652     PISSN: 02532964     EISSN: 12295949     Source Type: Journal    
DOI: 10.5012/bkcs.2009.30.9.1931     Document Type: Article
Times cited : (16)

References (34)
  • 1
    • 0002123299 scopus 로고    scopus 로고
    • For reviews on transition metal-catalyzed transfer hydrogenation, see
    • For reviews on transition metal-catalyzed transfer hydrogenation, see Noyori, R.; Hashiguchi, S. Acc. Chem. Res. 1997, 30, 97.
    • (1997) Acc. Chem. Res. , vol.30 , pp. 97
    • Noyori, R.1    Hashiguchi, S.2
  • 20
  • 24
    • 58149384265 scopus 로고    scopus 로고
    • These reactions could also be applied to transition metalcatalyzed Friedländer quinoline synthesis by oxidative cyclization of 2-aminobenzyl alcohol with ketones and secondary alcohols: and references cited therein
    • These reactions could also be applied to transition metalcatalyzed Friedländer quinoline synthesis by oxidative cyclization of 2-aminobenzyl alcohol with ketones and secondary alcohols: Cho, C.S.; Ren, W.X.; Yoon, N.S. J. Mol. Cat. A: Chem. 2009, 299, 117 and references cited therein.
    • (2009) J. Mol. Cat. A: Chem. , vol.299 , pp. 117
    • Cho, C.S.1    Ren, W.X.2    Yoon, N.S.3
  • 26
    • 75649119718 scopus 로고
    • For our reports using trialkylamines as an alkylating agent
    • For our reports using trialkylamines as an alkylating agent: Cho, C.S.; Oh, B.H.; Kim, J.S.; Kim, T.-J.; Shim, S.C. Chem. Commun. For our reports using trialkylamines as an alkylating agent. 2000, 1885.
    • (1885) Chem. Commun. , vol.2000
    • Cho, C.S.1    Oh, B.H.2    Kim, J.S.3    Kim, T.-J.4    Shim, S.C.5
  • 32
    • 75649091926 scopus 로고    scopus 로고
    • Note
    • 3N (0.2 mmol) and dioxane (5 mL). After the system was flushed with argon, the reaction mixture was allowed to react at 180 °C for 15 h. The reaction mixture was passed through a short silica gel column (ethyl acetate-hexane) to eliminate a ruthenium. Removal of the solvent left a crude mixture, which was separated by thin layer chromatography (silica gel, ethyl acetate-hexane mixture) to give trans-alkenes.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.