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Volumn 132, Issue 4, 2010, Pages 1188-1189

Intramolecular oxamidation of unsaturated O-alkyl hydroxamates: A remarkably versatile entry to hydroxy lactams

Author keywords

[No Author keywords available]

Indexed keywords

ALKYLATION; HYDROCARBONS; IODINE;

EID: 77950427980     PISSN: 00027863     EISSN: 15205126     Source Type: Journal    
DOI: 10.1021/ja9069997     Document Type: Article
Times cited : (126)

References (34)
  • 1
    • 3543085333 scopus 로고    scopus 로고
    • For reviews, see: a, Moss, R. A, Platz, M, Jones, M, Eds, Wiley-Interscience: Hoboken, NJ
    • For reviews, see: (a) Falvey, D. E. In Reactive Intermediate Chemistry; Moss, R. A., Platz, M., Jones, M., Eds.; Wiley-Interscience: Hoboken, NJ, 2004; p 593.
    • (2004) Reactive Intermediate Chemistry , pp. 593
    • Falvey, D.E.1
  • 4
    • 0026653993 scopus 로고    scopus 로고
    • For the intermolecular reaction of O-stabilized nitrenium ions with alkenes, see: (a) Vedejs, E.; Sano, H. Tetrahedron Lett. 1992, 33, 3261.
    • For the intermolecular reaction of O-stabilized nitrenium ions with alkenes, see: (a) Vedejs, E.; Sano, H. Tetrahedron Lett. 1992, 33, 3261.
  • 7
    • 47149103324 scopus 로고    scopus 로고
    • For the reaction of N-stabilized nitrenium (or diazenium) ions with alkenes, see: (a) Tsukamoto, M.; Murata, K.; Sakamoto, T.; Saito, S.; Kikugawa, Y. Heterocycles 2008, 75, 1133.
    • For the reaction of N-stabilized nitrenium (or diazenium) ions with alkenes, see: (a) Tsukamoto, M.; Murata, K.; Sakamoto, T.; Saito, S.; Kikugawa, Y. Heterocycles 2008, 75, 1133.
  • 11
    • 1542375289 scopus 로고    scopus 로고
    • For a review, see
    • For a review, see: Hu, X. E. Tetrahedron 2004, 60, 2701.
    • (2004) Tetrahedron , vol.60 , pp. 2701
    • Hu, X.E.1
  • 16
    • 84924255364 scopus 로고    scopus 로고
    • Taken in part from: Forslund, R. E. Ph.D. Thesis, University of Illinois at Chicago, 2003.
    • Taken in part from: Forslund, R. E. Ph.D. Thesis, University of Illinois at Chicago, 2003.
  • 17
    • 66149173396 scopus 로고    scopus 로고
    • For selected intramolecular alkene oxaminations, see: a
    • For selected intramolecular alkene oxaminations, see: (a) Donohoe, T. J.; Callens, C. K. A.; Thompson, A. L. Org. Lett. 2009, 11, 2305.
    • (2009) Org. Lett , vol.11 , pp. 2305
    • Donohoe, T.J.1    Callens, C.K.A.2    Thompson, A.L.3
  • 22
    • 69049094962 scopus 로고    scopus 로고
    • For Pb(IV)-mediated formation of bridged aziridines, see: Hu, H.; Faraldos, J. A.; Coates, R. M. J. Am. Chem. Soc. 2009, 131, 11998.
    • For Pb(IV)-mediated formation of bridged aziridines, see: Hu, H.; Faraldos, J. A.; Coates, R. M. J. Am. Chem. Soc. 2009, 131, 11998.
  • 23
    • 33947294377 scopus 로고
    • For β-opening of bicyclic aziridinium and epoxonium ions, see: a
    • For β-opening of bicyclic aziridinium and epoxonium ions, see: (a) Leonard, N. J.; Dixon, D. B. J. Org. Chem. 1970, 35, 3483.
    • (1970) J. Org. Chem , vol.35 , pp. 3483
    • Leonard, N.J.1    Dixon, D.B.2
  • 32
    • 84924230539 scopus 로고    scopus 로고
    • That in this case the approach of the alkene to the N-center may be intimately involved with, and assist in, the departure of the protonated trifluoroacetate group is not discounted.
    • That in this case the approach of the alkene to the N-center may be intimately involved with, and assist in, the departure of the protonated trifluoroacetate group is not discounted.
  • 34
    • 84924251156 scopus 로고    scopus 로고
    • Reductive cleavage of N-methoxy lactams to the corresponding lactams can be accomplished with range of reducing agents, including Mo(CO) 6 see ref 7, For experimental details, see the Supporting Information
    • 6 (see ref 7). For experimental details, see the Supporting Information.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.