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Synthesis of protected (purin-6-YL)glycines via Pd-catalyzed alpha-arylation of ethyl N-(diphenyl-methylidene)glycinate with 6-iodopurines
- 1.0100783 - UOCHB-X 20043008 RIV GB eng J - Journal Article
Hocek, Michal
Synthesis of protected (purin-6-YL)glycines via Pd-catalyzed alpha-arylation of ethyl N-(diphenyl-methylidene)glycinate with 6-iodopurines.
[Syntéza chráněných (purin-6-yl)glycinů Pd-katalyzovanou alfa-arylací ethyl N-(difenyl-methylidene)glycinatu s 6-jodopuriny.]
Heterocycles. Roč. 63, č. 7 (2004), s. 1673-1677. ISSN 0385-5414. E-ISSN 1881-0942
R&D Projects: GA ČR GA203/03/0035
Institutional research plan: CEZ:AV0Z4055905
Keywords : purines * cross-coupling
Subject RIV: CC - Organic Chemistry
Impact factor: 1.064, year: 2004
A synthesis of protected (purin-6-yl)glycines, potential building blocks of stable covalent peptide-nucleic acids conjugates, was achieved via Pd-catalyzed alpha-arylation of ethyl N-(diphenylmethylidene)glycinate with 6-iodopurine
Syntéza chráněných (purin-6-yl)glycinů, ponetciálních stavebních bloků pro stabilní konjugáty peptidů a nukleových kyselin, byla dosažena Pd-katalyzovanou alfa-arylací ethyl N-(difenylmethylidene)glycinatu s 6-jodopuriny
Permanent Link: http://hdl.handle.net/11104/0008272
Number of the records: 1