메뉴 건너뛰기




Volumn 132, Issue 29, 2010, Pages 10012-10014

Concerning the mechanism of the FeCl3-catalyzed α-oxyamination of aldehydes: Evidence for a non-SOMO activation pathway

Author keywords

[No Author keywords available]

Indexed keywords

ACTIVATION PATHWAY; ALCOHOL OXIDATION; CARBON-OXYGEN BONDS; ENAMINES; SIMPLE METALS;

EID: 77955779542     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja1043006     Document Type: Article
Times cited : (143)

References (31)
  • 23
    • 68049086802 scopus 로고    scopus 로고
    • Cyclopropyl radical ring opening/reclosure prior to productive bond formation has been observed previously. See: a
    • Cyclopropyl radical ring opening/reclosure prior to productive bond formation has been observed previously. See: (a) Benkovics, T.; Du, J.; Guzie, I. A.; Yoon, T. P. J. Org. Chem. 2009, 74, 5545.
    • (2009) J. Org. Chem. , vol.74 , pp. 5545
    • Benkovics, T.1    Du, J.2    Guzie, I.A.3    Yoon, T.P.4
  • 28
    • 77955796156 scopus 로고    scopus 로고
    • A background reaction with aldehyde and oxoammonium which can also be formed in situ from TEMPO was also observed
    • A background reaction with aldehyde and oxoammonium (which can also be formed in situ from TEMPO) was also observed.
  • 29
    • 77955802352 scopus 로고    scopus 로고
    • Use of 2 equiv of TEMPO allowed it to act as both the oxygen atom source and the stoichiometric reoxidant for iron see ref 1b
    • Use of 2 equiv of TEMPO allowed it to act as both the oxygen atom source and the stoichiometric reoxidant for iron (see ref 1b).
  • 31
    • 77955798489 scopus 로고    scopus 로고
    • Enamine/metal-TEMPO electron transfer followed by solvent-cage radical combination cannot be excluded on the basis of the studies herein
    • Enamine/metal-TEMPO electron transfer followed by solvent-cage radical combination cannot be excluded on the basis of the studies herein.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.