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Volumn 80, Issue 12, 2015, Pages 6025-6036

Constructing Quaternary Carbons from N -(Acyloxy)phthalimide Precursors of Tertiary Radicals Using Visible-Light Photocatalysis

Author keywords

[No Author keywords available]

Indexed keywords

ATOMS; CARBON; CATALYSIS; DICHLOROMETHANE; HYDROCARBONS; LIGHT; PHOTOCATALYSIS; RUBIDIUM COMPOUNDS; SUBSTITUTION REACTIONS;

EID: 84934921868     PISSN: 00223263     EISSN: 15206904     Source Type: Journal    
DOI: 10.1021/acs.joc.5b00795     Document Type: Article
Times cited : (207)

References (43)
  • 14
    • 84865435961 scopus 로고    scopus 로고
    • Similar photoredox catalysis conditions have been employed to initiate radical polymerization of methacrylates. See
    • Similar photoredox catalysis conditions have been employed to initiate radical polymerization of methacrylates. See: Fors, B. F.; Hawker, C. J. Angew. Chem., Int. Ed. 2012, 51, 8850-8853
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 8850-8853
    • Fors, B.F.1    Hawker, C.J.2
  • 20
    • 84872246918 scopus 로고    scopus 로고
    • Wille, U. Chem. Rev. 2013, 113, 813-853
    • (2013) Chem. Rev. , vol.113 , pp. 813-853
    • Wille, U.1
  • 25
    • 84878107052 scopus 로고    scopus 로고
    • For recent use of 4,4-dideuterio-Hantzsch esters in studies of reactions promoted by visible-light photoredox catalysis, see
    • For recent use of 4,4-dideuterio-Hantzsch esters in studies of reactions promoted by visible-light photoredox catalysis, see: Neumann, M.; Zeitler, K. Chem.-Eur. J. 2013, 19, 6950-6955
    • (2013) Chem.-Eur. J. , vol.19 , pp. 6950-6955
    • Neumann, M.1    Zeitler, K.2
  • 29
    • 77149120138 scopus 로고    scopus 로고
    • This potential is reported as -1.11 V vs ferrocene; see
    • This potential is reported as -1.11 V vs ferrocene; see: Zhu, X.-Q.; Tan, Y.; Cao, C.-T. J. Phys. Chem. B 2010, 114, 2058-2075
    • (2010) J. Phys. Chem. B , vol.114 , pp. 2058-2075
    • Zhu, X.-Q.1    Tan, Y.2    Cao, C.-T.3
  • 30
    • 0001112346 scopus 로고
    • Okada reports reduction potentials in the range of -1.28 to -1.37 V (vs SCE) for three N -(acyloxy)phthalimides in acetonitrile, see
    • Okada reports reduction potentials in the range of -1.28 to -1.37 V (vs SCE) for three N -(acyloxy)phthalimides in acetonitrile, see: Okada, K.; Okamoto, K.; Oda, M. J. Am. Chem. Soc. 1988, 110, 8736-8738
    • (1988) J. Am. Chem. Soc. , vol.110 , pp. 8736-8738
    • Okada, K.1    Okamoto, K.2    Oda, M.3
  • 31
    • 35449001112 scopus 로고    scopus 로고
    • Electron Transfer, Bond Breaking and Bond Formation
    • In; Tidwell, T. T. Academic: New York, Vol.
    • Savéant, J.-M. Electron Transfer, Bond Breaking and Bond Formation. In Advances in Physical Organic Chemistry; Tidwell, T. T., Ed.; Academic: New York, 2000, Vol. 35, pp 117-192.
    • (2000) Advances in Physical Organic Chemistry , vol.35 , pp. 117-192
    • Savéant, J.-M.1
  • 32
    • 84934994774 scopus 로고    scopus 로고
    • Owing to the low barrier for decarboxylation of carboxy radicals, K may well not be an intermediate, with decarboxylation occurring at the same time as fragmentation of the N-O bond.
    • Owing to the low barrier for decarboxylation of carboxy radicals, K may well not be an intermediate, with decarboxylation occurring at the same time as fragmentation of the N-O bond.
  • 35
    • 84880013743 scopus 로고    scopus 로고
    • 2+ photocatalyzed ketone-alkene coupling, see
    • 2+ photocatalyzed ketone-alkene coupling, see: Taratino, K. T.; Liu, P.; Knowles, R. R. J. Am. Chem. Soc. 2013, 135, 10022-10025
    • (2013) J. Am. Chem. Soc. , vol.135 , pp. 10022-10025
    • Taratino, K.T.1    Liu, P.2    Knowles, R.R.3
  • 39
    • 84934891027 scopus 로고    scopus 로고
    • Reference 32a.
    • Reference 32a.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.