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Volumn 18, Issue , 1989, Pages 187-208

Centenary Lecture. Chemical multiplication of chirality: Science and applications

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Indexed keywords


EID: 34247236924     PISSN: 03060012     EISSN: None     Source Type: Journal    
DOI: 10.1039/CS9891800187     Document Type: Review
Times cited : (432)

References (65)
  • 1
    • 0001736112 scopus 로고    scopus 로고
    • For the present state of this subject, ed. R. Scheffold, Springer vrlag, Berlin
    • For the present state of this subject, see R. Noyori and M. Kitamura, in 'Modern Synthetic Methods 1989', ed. R. Scheffold, Springer vrlag, Berlin, p. 115.
    • 'Modern Synthetic Methods 1989' , pp. 115
    • Noyori, R.1    Kitamura, M.2
  • 18
    • 0002260975 scopus 로고
    • Pertinent reviews, ed. J. D. Morrison, Academic Press, New York, Chapter 2
    • Pertinent reviews: J. Halpern, in 'Asymmetric Synthesis', Vol. 5, ed. J. D. Morrison, Academic Press, New York, 1985, Chapter 2
    • (1985) 'Asymmetric Synthesis' , vol.5
    • Halpern, J.1
  • 23
    • 84985560333 scopus 로고
    • For a review on stereoselective olefin hydrogenation directed by functional groups
    • For a review on stereoselective olefin hydrogenation directed by functional groups, see J. M. Brown, Angew. Chem., Int. Ed. Engl., 1987, 26, 190.
    • (1987) Angew. Chem., Int. Ed. Engl , vol.26 , pp. 190
    • Brown, J.M.1
  • 26
    • 0001789053 scopus 로고
    • For synthesis via stoicheiometric enantioselective alkylation
    • For synthesis via stoicheiometric enantioselective alkylation, see A. I. Meyers, Aldrichimica Acta, 1985, 18, 59.
    • (1985) Aldrichimica Acta , vol.18 , pp. 59
    • Meyers, A.I.1
  • 38
    • 0001206269 scopus 로고
    • R. Noyori, Chimia, 1988, 42, 215.
    • (1988) Chimia , vol.42 , pp. 215
    • Noyori, R.1
  • 43
    • 84944147464 scopus 로고
    • Vol. 2A, ed. J. D. Morrison, Academic Press, New York, Chapter 6
    • G. Soladie, in 'Asymmetric Synthesis', Vol. 2A, ed. J. D. Morrison, Academic Press, New York, 1983, Chapter 6
    • (1983) 'Asymmetric Synthesis'
    • Soladie, G.1
  • 58
  • 63
    • 33845379409 scopus 로고
    • A planar bicyclic transition state has been proposed for reaction of methyllithium dimer and formaldehyde
    • A planar bicyclic transition state has been proposed for reaction of methyllithium dimer and formaldehyde: E. Kaufmann, P. von R. Schleyer, K. N. Houk, and Y.-D. Wu, J. Am. Chem. Soc, 1985, 107, 5560.
    • (1985) J. Am. Chem. Soc , vol.107 , pp. 5560
    • Kaufmann, E.1    Schleyer, P.V.2    Houk, K.N.3    Wu, Y.-D.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.