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Volumn 1988, Issue 1, 1988, Pages 73-76

A facile and versatile synthesis of 2-Substituted tryptophans as N α-tert-Butyloxycarbonyl derivatives

Author keywords

[No Author keywords available]

Indexed keywords

TRYPTOPHAN DERIVATIVE;

EID: 0023721224     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-1988-27471     Document Type: Article
Times cited : (22)

References (36)
  • 1
    • 85082866006 scopus 로고    scopus 로고
    • New address for correspondence: Smith Kline and French LaboraÂtories, 709 Swedeland Road, King of Prussia, PA 19406-2799, USA
    • New address for correspondence: Smith Kline and French LaboraÂtories, 709 Swedeland Road, King of Prussia, PA 19406-2799, USA.
  • 2
    • 85082856718 scopus 로고    scopus 로고
    • Present address: Zoecon Research Institute, Sandoz Crop ProtecÂtion Corp. 975 California Avenue, Palo Alto, CA 94304, USA
    • Present address: Zoecon Research Institute, Sandoz Crop ProtecÂtion Corp., 975 California Avenue, Palo Alto, CA 94304, USA.
  • 10
    • 0007444488 scopus 로고
    • Like other 2-hydroxyindoles, 2-hydroxytryptophan exists excluÂsively in the oxo form β-(2-oxo-2, 3-dihydroindolyl)alanine, see
    • Like other 2-hydroxyindoles, 2-hydroxytryptophan exists excluÂsively in the oxo form β-(2-oxo-2, 3-dihydroindolyl)alanine, see Cornforth, J. W., Dalgliesh, C. E., Neuberger, A. Biochem. J. 1951, 48, 598.
    • (1951) Biochem. J , vol.48 , pp. 598
    • Cornforth, J.W.1    Dalgliesh, C.E.2    Neuberger, A.3
  • 22
    • 0000276974 scopus 로고
    • Racemic 2-ethylthio-, N∗-hydroxytryptophan ethyl ester has been prepared from 3-ethylthioindole by this method. The concurrent rearomatization of the indole nucleus and the attachment of the 2-thioether involved the migration of an alkylthio group. See
    • Racemic 2-ethylthio-, N∗-hydroxytryptophan ethyl ester has been prepared from 3-ethylthioindole by this method. The concurrent rearomatization of the indole nucleus and the attachment of the 2-thioether involved the migration of an alkylthio group. See: Plate, R., Ottenheijm, H.C.J., Nivard, R.J.F. J. Org. Chem. 1984, 49, 540.
    • (1984) J. Org. Chem , vol.49 , pp. 540
    • Plate, R.1    Ottenheijm, H.C.J.2    Nivard, R.J.F.3
  • 24
    • 85082868588 scopus 로고    scopus 로고
    • Instead of the Boc group, other protection groups, such as the Z group, may be used
    • Instead of the Boc group, other protection groups, such as the Z group, may be used.
  • 27
    • 85082846909 scopus 로고
    • Sterling Drug. Inc. C.A. 1970, 72, 66807
    • Bell, M. R. D.O.S. 1908541 (1969), Sterling Drug. Inc.; C.A. 1970, 72, 66807.
    • (1969) D.O.S. 1908541
    • Bell, M.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.