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Volumn , Issue 13, 2003, Pages 2443-2453

Diastereoselective synthesis of 1-benzyltetrahydroisoquinoline derivatives from amino acids by 1,4 chirality transfer

Author keywords

Alkaloids; Amino acids; Asymmetric synthesis

Indexed keywords

1 BENZYLTETRAHYDROISOQUINOLINE DERIVATIVE; ALANINE; AMIDE; AMINO ACID; KETOAMIDE; PHENYLALANINE; PROLINE; QUINOLINE DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037925194     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/ejoc.200200705     Document Type: Article
Times cited : (19)

References (43)
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    • Lundstorom, J.1
  • 2
    • 77957038402 scopus 로고
    • (Ed.: A. Brossi), Academic Press, New York
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  • 3
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    • (Ed.: G. A. Cordell), Academic Press, San Diego
    • A. Brossi, The Alkaloids, Vol. 43 (Ed.: G. A. Cordell), Academic Press, San Diego, 1993, pp. 119-183.
    • (1993) The Alkaloids , vol.43 , pp. 119-183
    • Brossi, A.1
  • 6
    • 4243241249 scopus 로고
    • and references therein
    • E. D. Cox, J. M. Cook, Chem. Rev. 1995, 95, 1797-1842 and references therein.
    • (1995) Chem. Rev. , vol.95 , pp. 1797-1842
    • Cox, E.D.1    Cook, J.M.2
  • 20
    • 8344249465 scopus 로고    scopus 로고
    • and references therein
    • F. J. Sardina, H. Rapoport, Chem. Rev. 1996, 96, 1825-1872 and references therein.
    • (1996) Chem. Rev. , vol.96 , pp. 1825-1872
    • Sardina, F.J.1    Rapoport, H.2
  • 21
    • 0037944185 scopus 로고    scopus 로고
    • and references therein
    • E. N. Jacobsen, Synthesis 1996, 792-815 and references therein.
    • (1996) Synthesis , pp. 792-815
    • Jacobsen, E.N.1
  • 31
    • 77957077000 scopus 로고
    • (Ed.: A. Brossi), Academic Press, New York
    • H. Hiemstra, W. N. Speckamp, in The Alkaloids (Ed.: A. Brossi), Academic Press, New York, 1988, Vol. 32, pp. 271-339.
    • (1988) The Alkaloids , vol.32 , pp. 271-339
    • Hiemstra, H.1    Speckamp, W.N.2
  • 36
    • 0037606131 scopus 로고    scopus 로고
    • note
    • The numbering mode for compounds 6 in Scheme 1 is shown in Figure 1 and is based on IUPAC rules.
  • 37
    • 0037606132 scopus 로고    scopus 로고
    • note
    • We thank the referee of this paper for this suggestion.
  • 38
    • 0037944187 scopus 로고    scopus 로고
    • note
    • The ratio of S:R ≥ 99.5:0.5 was determined on a ChiraDex column (Merck).
  • 39
    • 0038281465 scopus 로고    scopus 로고
    • note
    • The numbering scheme of 12a and 12b is shown in Figure 2 and is based on IUPAC rules.
  • 41
    • 0037944188 scopus 로고    scopus 로고
    • note
    • -1.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.