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Volumn 64, Issue , 2004, Pages 605-658

β-lactones: Intermediates for natural product total synthesis and new transformations

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EID: 17044405496     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/REV-04-SR(P)3     Document Type: Article
Times cited : (125)

References (133)
  • 1
    • 84980114758 scopus 로고
    • Einhorn A. Ber. 16 (1883) 2208
    • (1883) Ber. , vol.16 , pp. 2208
    • Einhorn, A.1
  • 3
    • 0037539910 scopus 로고    scopus 로고
    • For a review of ketene chemistry, which includes recent advances in the catalytic, asymmetric synthesis of β lactones, see
    • For a review of ketene chemistry, which includes recent advances in the catalytic, asymmetric synthesis of β lactones, see. Calter M.A., and Orr R.K. Tetrahedron 59 (2003) 3545
    • (2003) Tetrahedron , vol.59 , pp. 3545
    • Calter, M.A.1    Orr, R.K.2
  • 7
    • 0033859279 scopus 로고    scopus 로고
    • For an excellent review describing synthetic and biological studies of lactacystin, see
    • For an excellent review describing synthetic and biological studies of lactacystin, see. Masse C., Morgan J., Adams J., and Panek J. Eur. J. Org. Chem. (2000) 2513
    • (2000) Eur. J. Org. Chem. , pp. 2513
    • Masse, C.1    Morgan, J.2    Adams, J.3    Panek, J.4
  • 10
    • 37049094683 scopus 로고
    • Acids were found to induce changes from retention to inversion of configuration of two distinct cis-β-lactones
    • Acids were found to induce changes from retention to inversion of configuration of two distinct cis-β-lactones. Mulzer J., and Zippel M. Chem. Commun. (1981) 891
    • (1981) Chem. Commun. , pp. 891
    • Mulzer, J.1    Zippel, M.2
  • 58
    • 33747109188 scopus 로고
    • The Chemical Society, Burlington House, New York
    • A Specialist Periodical Report, Biosynthesis Vol. 1-5 (1970), The Chemical Society, Burlington House, New York
    • (1970) A Specialist Periodical Report, Biosynthesis , vol.1-5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.