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Mendeleev Communications, 2014, Volume 24, Issue 1, Pages 35–36
DOI: https://doi.org/10.1016/j.mencom.2013.12.011
(Mi mendc2464)
 

This article is cited in 16 scientific papers (total in 16 papers)

Communications

Novel synthetic routes to N-(2-amino-9H-purin-6-yl)-substituted amino acids

A. Yu. Vigorov, V. P. Krasnov, D. A. Gruzdev, A. A. Men'shikova, A. M. Demin, G. L. Levit, V. N. Charushin

I.Ya. Postovsky Institute of Organic Synthesis, Ural Branch of the Russian Academy of Sciences, Ekaterinburg, Russian Federation
Abstract: Reaction of N2-protected 2-amino-6-chloropurine with tert-butyl (S)-phenylalaninate, (R)- and (S)-valinates followed by deprotection affords 2-aminopurines bearing at 6-position the corresponding amino acid moieties, whose chiral centre is partially racemized.
Bibliographic databases:
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (317.3 Kb)


Citation: A. Yu. Vigorov, V. P. Krasnov, D. A. Gruzdev, A. A. Men'shikova, A. M. Demin, G. L. Levit, V. N. Charushin, “Novel synthetic routes to N-(2-amino-9H-purin-6-yl)-substituted amino acids”, Mendeleev Commun., 24:1 (2014), 35–36
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  • https://www.mathnet.ru/eng/mendc/v24/i1/p35
  • This publication is cited in the following 16 articles:
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