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Development of metallocomplex amino acids synthons for the asymmetric preparation of alfa-amino acids by stereoselective introduction of a side chain. Evaluation of the model asymmetric preparation of alanine and beta-C-13 monolabelled alfa-aminoisobutyric acid

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216275%3A25310%2F10%3A39881300" target="_blank" >RIV/00216275:25310/10:39881300 - isvavai.cz</a>

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Development of metallocomplex amino acids synthons for the asymmetric preparation of alfa-amino acids by stereoselective introduction of a side chain. Evaluation of the model asymmetric preparation of alanine and beta-C-13 monolabelled alfa-aminoisobutyric acid

  • Original language description

    The evaluation of 11 new metallocomplex alanine synthons bearing C-2-symmetric benzyl groups with electron-donating and withdrawing substituents is described. alpha-Methylated glycine synthons (alanine complexes) were evaluated alongside alanine synthonsin order to obtain a deeper understanding of the relationship between their structures and stereochemistry of monoalkylated products and to choose several candidates for their further tests for stereospecific preparation of 6-[F-18]FDOPA. Glycine-derived analogues of the complexes 3-5 are the best candidates for the development of a 6-[F-18]FDOPA preparation procedure. In the model epimerisation reaction they demonstrated the best performance, much better compared to the previously described compound 2. Complexes 3, 5 and 8 are the best in asymmetric preparation of beta-C-13 monolabelled alpha-aminoisobutyric acid. They have to be tested in the preparation of alpha-methyl amino acids like 6-[F-18]-alpha-methylDOPA and 2-[F-18]-alpha-me

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>x</sub> - Unclassified - Peer-reviewed scientific article (Jimp, Jsc and Jost)

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)

Others

  • Publication year

    2010

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Radioanalytical and Nuclear Chemistry

  • ISSN

    0236-5731

  • e-ISSN

  • Volume of the periodical

    285

  • Issue of the periodical within the volume

    3

  • Country of publishing house

    NL - THE KINGDOM OF THE NETHERLANDS

  • Number of pages

    6

  • Pages from-to

  • UT code for WoS article

    000281089300030

  • EID of the result in the Scopus database