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Volumn 6, Issue 2, 2004, Pages 257-260

Efficient Oxidative Radical Cyclizations of Ester Enolates with Carbocation Desilylation as Termination: Synthesis of Cyclopentanoid Monoterpenes and Analogues

Author keywords

[No Author keywords available]

Indexed keywords

CATION; CYCLOHEXANE DERIVATIVE; CYCLOPENTANE DERIVATIVE; CYCLOPENTENE DERIVATIVE; ESTER DERIVATIVE; FERROCENE DERIVATIVE; FERROCENIUM HEXAFLUOROPHOSPHATE; LACTONE DERIVATIVE; OXIDIZING AGENT; RADICAL; SILANE DERIVATIVE; TERPENE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0842328413     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol036233n     Document Type: Article
Times cited : (35)

References (25)
  • 7
  • 14
    • 0034545467 scopus 로고    scopus 로고
    • For a review, see: Moeller, K. D. Tetrahedron 2000, 56, 9527-9554.
    • (2000) Tetrahedron , vol.56 , pp. 9527-9554
    • Moeller, K.D.1
  • 15
    • 0030797910 scopus 로고    scopus 로고
    • For synthetic approaches, see: (a) Nangia, A.; Prasuna, G.; Rao, P. B. Tetrahedron 1997, 53, 14507-14545. (b) Thomas, A. F.; Bessiere, Y. In The Total Synthesis of Natural Products; ApSimon, J., Ed.; Wiley: New York, 1988; Vol. 7, pp 275-454.
    • (1997) Tetrahedron , vol.53 , pp. 14507-14545
    • Nangia, A.1    Prasuna, G.2    Rao, P.B.3
  • 16
    • 85050056091 scopus 로고
    • ApSimon, J., Ed.; Wiley: New York
    • For synthetic approaches, see: (a) Nangia, A.; Prasuna, G.; Rao, P. B. Tetrahedron 1997, 53, 14507-14545. (b) Thomas, A. F.; Bessiere, Y. In The Total Synthesis of Natural Products; ApSimon, J., Ed.; Wiley: New York, 1988; Vol. 7, pp 275-454.
    • (1988) The Total Synthesis of Natural Products , vol.7 , pp. 275-454
    • Thomas, A.F.1    Bessiere, Y.2
  • 18
    • 0002657532 scopus 로고    scopus 로고
    • Oxidation potentials of some silylated radicals compared to alkyl radicals, see: Zhang, S.; Bordwell, F. G. J. Org. Chem. 1996, 61, 51-54.
    • (1996) J. Org. Chem. , vol.61 , pp. 51-54
    • Zhang, S.1    Bordwell, F.G.2
  • 19
    • 0842300568 scopus 로고    scopus 로고
    • note
    • The configuration of 10c was assigned on the basis of NOE experiments (Supporting Information).
  • 21
    • 0842321999 scopus 로고    scopus 로고
    • note
    • This alcohol may be useful for the synthesis of other iridoids.
  • 25
    • 1342276877 scopus 로고
    • Compare: (a) Fleming, I.; Terrett, N. K. J. Chem. Soc., Perkin Trans. 1 1998, 2645-2649. (b) Uyehara, T.; Shida, N.; Yamamoto, Y. J. Org. Chem. 1992, 57, 3139-3145.
    • (1992) J. Org. Chem. , vol.57 , pp. 3139-3145
    • Uyehara, T.1    Shida, N.2    Yamamoto, Y.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.