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Number of results

Journal

2005 | 3 | 1 | 118-136

Article title

Studies on stereoselective approaches to β-carboline derivatives

Content

Title variants

Languages of publication

EN

Abstracts

EN
Transformation of β-carboline derivatives into optically active entities were studied and the de and ee values of the resulted compounds were detected.

Publisher

Journal

Year

Volume

3

Issue

1

Pages

118-136

Physical description

Dates

published
1 - 3 - 2005
online
1 - 3 - 2005

Contributors

  • Department of Organic Chemistry, University of Technology and Economics, Gellért tér 4, H-1111, Budapest, Hungary
  • Research Group for Alkaloid Chemistry, Hungarian Academy of Sciences, Gellért tér 4, Hungary
author
  • Department of Organic Chemistry, University of Technology and Economics, Gellért tér 4, H-1111, Budapest, Hungary
  • Department of Organic Chemistry, University of Technology and Economics, Gellért tér 4, H-1111, Budapest, Hungary
author
  • Department of Organic Chemistry, University of Technology and Economics, Gellért tér 4, H-1111, Budapest, Hungary
  • Central Research Center, Hungarian Academy of Sciences, P.O. Box 17, H-1525, Budapest, Hungary

References

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  • [21] H.J.R. Lucas and W. Baumgarten: “The reduction of tartaric acid”, J. Am. Chem. Soc., Vol. 63, (1941), pp. 1653–1657. http://dx.doi.org/10.1021/ja01851a043[Crossref]
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  • [32] K. Tomohiko, N. Masako, Y. Hitoshi, H. Mariko and H. Tohru: “Alkylation of 3,4-dihydro-β-carboline”, Chem. Pharm. Bull., Vol. 41, (1993), pp. 287–291.
  • [33] Z. Czarnocki, D.B. MacLean and W.A. Szarek: “Diastereoselective reduction of derivatives of 3,4-dihydro-1-methylidene-2-tartaroylisoquinoline”, Heterocycles, Vol. 34, (1992), pp. 943–953. http://dx.doi.org/10.3987/COM-91-5959[Crossref]

Document Type

Publication order reference

Identifiers

YADDA identifier

bwmeta1.element.-psjd-doi-10_2478_BF02476243
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