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Volumn 18, Issue 24, 1999, Pages 5017-5021

Synthesis and Atropo-diastereoselective Ring Cleavage of a [Cp*Ru]-Complexed Biaryl Lactone: Experimental and Computational Investigations

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Indexed keywords


EID: 0001282681     PISSN: 02767333     EISSN: None     Source Type: Journal    
DOI: 10.1021/om9906520     Document Type: Article
Times cited : (10)

References (38)
  • 16
    • 0347498897 scopus 로고    scopus 로고
    • note
    • For the investigations on diastereoselective ring cleavage reactions described here, it was sufficient to prepare the complex 5b in a racemic form.
  • 20
    • 0346237918 scopus 로고    scopus 로고
    • note
    • The relative configuration at the biaryl axis was determined by NOE/ROE experiments, showing a correlation between the hydroxy proton and the methyl group protons of the Cp* ligand.
  • 30
    • 0347498898 scopus 로고    scopus 로고
    • note
    • The use of the older Gaussian 92 program package, by contrast, showed only large values of the Fukui function in the region of the metal center and the Michael acceptor and phenylogous Michael acceptor positions.
  • 36
    • 0002553839 scopus 로고
    • Labanowski, J., Andzelm, J., Eds.; Springer: New York, DGAUSS is part of the UniChem-Programs of Cray Research, Inc., Eagan, MN
    • Andzelm, J. In Density Functional Methods in Chemistry; Labanowski, J., Andzelm, J., Eds.; Springer: New York, 1991; p 155. DGAUSS is part of the UniChem-Programs of Cray Research, Inc., Eagan, MN.
    • (1991) Density Functional Methods in Chemistry , pp. 155
    • Andzelm, J.1
  • 38
    • 85021033598 scopus 로고    scopus 로고
    • Tripos Associates: 1699 St. Hanley Road, Suite 303, St. Louis, MO, 63114
    • SYBYL 6.2; Tripos Associates: 1699 St. Hanley Road, Suite 303, St. Louis, MO, 63114.
    • SYBYL 6.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.