Email this article Diastereotopic derivatives of chiral alkoxyisoindolinones
- Authors: Grigoreva T.A.1, Garabadzhiu A.V.1, Tribulovich V.G.1
-
Affiliations:
- St. Petersburg State Institute of Technology (Technical University)
- Issue: Vol 86, No 11 (2016)
- Pages: 2454-2461
- Section: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/216503
- DOI: https://doi.org/10.1134/S1070363216110098
- ID: 216503
Cite item
Open Access
Access granted
Subscription Access
Abstract
A method for synthesis of 2,3-substituted 3-hydroxyisoindolin-1-one acyl derivatives, modified reactivators of tumor suppressor protein p53, was developed; these compounds were synthesized and characterized. It was shown that diastereomeric esters of Boc-N-protected amino acids, unlike esters with a free amino group, can be preparatively isolated by flash chromatography using achiral media.
Keywords
About the authors
T. A. Grigoreva
St. Petersburg State Institute of Technology (Technical University)
Author for correspondence.
Email: rozentatiana@gmail.com
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
A. V. Garabadzhiu
St. Petersburg State Institute of Technology (Technical University)
Email: rozentatiana@gmail.com
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
V. G. Tribulovich
St. Petersburg State Institute of Technology (Technical University)
Email: rozentatiana@gmail.com
Russian Federation, Moskovskii pr. 26, St. Petersburg, 190013
Supplementary files
