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Volumn 694, Issue 24, 2009, Pages 3837-3839

Photo-allylation and photo-benzylation of carbonyl compounds using organotrifluoroborate reagents

Author keywords

Allylation; Benzylation; Carbonyl compound; Electron transfer; Organotrifluoroborate; Photoreaction

Indexed keywords

ALLYLATION; BENZYLATION; CARBONYL COMPOUND; ELECTRON TRANSFER; ORGANOTRIFLUOROBORATE; PHOTOREACTION;

EID: 70349972593     PISSN: 0022328X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jorganchem.2009.08.011     Document Type: Article
Times cited : (31)

References (31)
  • 5
    • 0003702881 scopus 로고
    • Mariano P.S. (Ed), JAI Press, Stamford
    • In: Mariano P.S. (Ed). Advances in Electron Transfer Chemistry vols. 1-6 (1991-1999), JAI Press, Stamford
    • (1991) Advances in Electron Transfer Chemistry , vol.1-6
  • 19
    • 33845378390 scopus 로고
    • As a pioneering work, Lan and Schuster reported photo-induced substitution of aromatic cyanides using benzyltriphenylborate
    • As a pioneering work, Lan and Schuster reported photo-induced substitution of aromatic cyanides using benzyltriphenylborate. Lan J.Y., and Schuster G.B. J. Am. Chem. Soc. 107 (1985) 6710
    • (1985) J. Am. Chem. Soc. , vol.107 , pp. 6710
    • Lan, J.Y.1    Schuster, G.B.2
  • 20
    • 70349926501 scopus 로고    scopus 로고
    • Reduction potentials of the carbonyl compounds were measured as a DPV peak value in acetonitrile with reference of Fc+/Fc. Redox potential of Fc+/Fc was reportedly 0.40 V vs. SCE in acetonitrile [8b
    • +/Fc was reportedly 0.40 V vs. SCE in acetonitrile [8b]
  • 30
    • 70349916980 scopus 로고    scopus 로고
    • note
    • ox (V vs. SCE) of the borates were determine as in Ref. [8a]. 1: +1.10, 2: +0.93, 8: +0.76, 9: +0.62.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.