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Volumn 60, Issue 15, 2004, Pages 3427-3432

Reinvestigation of the synthetic and mechanistic aspects of Mn(III) acetate mediated oxidation of enones

Author keywords

Alkenes; Enones; Mn(OAc)3; Oxidation

Indexed keywords

ACETIC ACID; KETONE DERIVATIVE; MANGANESE DERIVATIVE;

EID: 1642326527     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tet.2004.02.039     Document Type: Article
Times cited : (29)

References (28)
  • 10
    • 33947329731 scopus 로고
    • 3 together with the rate of the reaction. However, yields were relatively unaffected:
    • 3 together with the rate of the reaction. However, yields were relatively unaffected: Bush J.B. Jr., Finkbeiner H. J. Am. Chem. Soc. 90:1968;5903.
    • (1968) J. Am. Chem. Soc. , vol.90 , pp. 5903
    • Bush Jr., J.B.1    Finkbeiner, H.2
  • 23
    • 0242391636 scopus 로고
    • 3 oxidation of saturated ketones provide complex mixtures:
    • 3 oxidation of saturated ketones provide complex mixtures: Okano M., Aratani T. Bull. Chem. Soc. Jpn. 49:1976;2811.
    • (1976) Bull. Chem. Soc. Jpn. , vol.49 , pp. 2811
    • Okano, M.1    Aratani, T.2
  • 24
    • 0029869740 scopus 로고    scopus 로고
    • Snider stated that oxidation of α′-keto radical derived from enones is a very fast process relative to oxidation of radicals derived from saturated ketones. Attempted alkene addition to an enone in the presence of 1-octene provided only acetoxylation and oligomer: (a)
    • Snider stated that oxidation of α′-keto radical derived from enones is a very fast process relative to oxidation of radicals derived from saturated ketones. Attempted alkene addition to an enone in the presence of 1-octene provided only acetoxylation and oligomer: (a) Snider B.B., Kiselgof E.Y. Tetrahedron. 52:1996;6073.
    • (1996) Tetrahedron , vol.52 , pp. 6073
    • Snider, B.B.1    Kiselgof, E.Y.2
  • 25
    • 0030858681 scopus 로고    scopus 로고
    • Successful intermolecular addition of enones to alkenes providing dihydrobenzofurans was reported: (b)
    • Successful intermolecular addition of enones to alkenes providing dihydrobenzofurans was reported: (b) Snider B.B., Han L., Xie C. J. Org. Chem. 62:1997;6978.
    • (1997) J. Org. Chem. , vol.62 , pp. 6978
    • Snider, B.B.1    Han, L.2    Xie, C.3
  • 26
    • 0345731482 scopus 로고    scopus 로고
    • 3 to mediate reactions that is possibly based on reductive elimination of arylmanganese intermediates:
    • 3 to mediate reactions that is possibly based on reductive elimination of arylmanganese intermediates: Demir A.S., Reis Ö., Emrullahoglu M. J. Org. Chem. 68:2003;10130.
    • (2003) J. Org. Chem. , vol.68 , pp. 10130
    • Demir, A.S.1    Reis, Ö.2    Emrullahoglu, M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.