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Volumn 82, Issue 2, 2010, Pages 1327-1336

Efficient phenolic oxidations to construct orttho-spirolactone structures using oxo-bridged hypervalent iodine(III) compound

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EID: 79952766417     PISSN: 03855414     EISSN: 18810942     Source Type: Journal    
DOI: 10.3987/COM-10-S(E)79     Document Type: Article
Times cited : (19)

References (31)
  • 1
    • 0001213492 scopus 로고    scopus 로고
    • Chem. Rev
    • Recent reviews and publications: a) P. J. Stang and V. V. Zhdankin, Chem. Rev, 1996, 96, 1123;
    • (1996) , vol.96 , pp. 1123
    • Stang, P.J.1    Zhdankin, V.V.2
  • 5
    • 79952768276 scopus 로고    scopus 로고
    • Hypervalent Iodine Chemistry; T. Wirth, Ed.; Springer-Verlag: Berlin, Heidelberg, 2003
    • e) Hypervalent Iodine Chemistry; T. Wirth, Ed.; Springer-Verlag: Berlin, Heidelberg, 2003;
  • 20
    • 0034597522 scopus 로고    scopus 로고
    • For recent reports of natural product syntheses containing the ortho-spirolactone structures, see: a) C. Cox and S. J. Danishefsky, Org. Lett., 2000, 2, 3493;
    • (2000) Org. Lett. , vol.2 , pp. 3493
    • Cox, C.1    Danishefsky, S.J.2
  • 22
    • 0344792636 scopus 로고    scopus 로고
    • Angew. Chem. Int. Ed., 2003, 42, 5629
    • (2003) , vol.42 , pp. 5629
    • Ed, Int.1
  • 26
    • 0001677413 scopus 로고    scopus 로고
    • In contrast, the cyclohexa-2,4-dienones obtained from the oxidations of simple phenol carboxylic acids are generally quite reactive and have high propensity toward self-dimerization through the Diels-Alder process. For selected example, see: I. Drutu, J. T. Njardarson, and J. L. Wood, Org. Lett., 2002, 4, 493.
    • (2002) Org. Lett. , vol.4 , pp. 493
    • Drutu, I.1    Njardarson, J.T.2    Wood, J.L.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.