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Volumn , Issue 4, 1996, Pages 489-499

Experimental and theoretical studies of the internal stereodifferentiation occurring during the lithiation of β-stereogenic alkyl carbamates. Kinetic resolutions by (-)-sparteine-mediated deprotonation

Author keywords

( ) Sparteine; Alkyl carbamates; Calculations, PM3; Diastereoselective deprotonation; Kinetic resolution

Indexed keywords


EID: 33749124991     PISSN: 09473440     EISSN: None     Source Type: Journal    
DOI: 10.1002/jlac.199619960408     Document Type: Article
Times cited : (12)

References (51)
  • 1
    • 0000253140 scopus 로고
    • For some reviews see: [1a] P. Beak, D. B. Reitz, Chem. Rev. 1978, 78, 275-316.
    • (1978) Chem. Rev. , vol.78 , pp. 275-316
    • Beak, P.1    Reitz, D.B.2
  • 23
    • 33749121018 scopus 로고    scopus 로고
    • Alcohol (S)-(-)-7a obtained from Merck
    • Alcohol (S)-(-)-7a obtained from Merck.
  • 24
    • 85088226316 scopus 로고    scopus 로고
    • 20 = +20.8, c = 1.1, acetone)
    • 20 = +20.8, c = 1.1, acetone).
  • 25
    • 85088224440 scopus 로고    scopus 로고
    • 20 = +76.3, c = 1.1, anhydrous ethanol)
    • 20 = +76.3, c = 1.1, anhydrous ethanol).
  • 28
    • 33749139371 scopus 로고
    • Ph. D. Thesis, University of Münster
    • J. Haller, Ph. D. Thesis, University of Münster, 1995.
    • (1995)
    • Haller, J.1
  • 42
    • 33749135095 scopus 로고    scopus 로고
    • For the sake of clarity of the drawings, not the removal of the other diastereotopic proton in the same enantiomer was simulated, but the inducing chiral center was inverted
    • For the sake of clarity of the drawings, not the removal of the other diastereotopic proton in the same enantiomer was simulated, but the inducing chiral center was inverted.
  • 49
    • 0004175094 scopus 로고
    • W. A. Benjamin, Inc., New York
    • H. C. Brown, Hydroboration, W. A. Benjamin, Inc., New York, 1962, p. 98.
    • (1962) Hydroboration , pp. 98
    • Brown, H.C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.