Separation of racemic salycylaldehydes containing isobornyl substituent using (R)-1-phenylethylamine View Full Text


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Article Info

DATE

2010-05

AUTHORS

E. V. Buravlev, I. Yu. Chukicheva, F. M. Dolgushin, A. V. Kuchin

ABSTRACT

Racemic salicylaldehydes containing isobornyl substituent were separated by their conversion into diastereomers by the reaction with (R)-1-phenylethylamine. The absolute configuration of the intermediate Schiff bases and separated aldehyde eneatiomers was established by XRD analysis.

PAGES

649-654

References to SciGraph publications

  • 2008-03. Antithrombogenic and antiplatelet activity of optho-isobornyl phenol derivative in BULLETIN OF EXPERIMENTAL BIOLOGY AND MEDICINE
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1134/s1070428010050088

    DOI

    http://dx.doi.org/10.1134/s1070428010050088

    DIMENSIONS

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