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Synthesis of C-2-symmetrical [1,1 '-binaphthalene]-2,2 '-diamines with additional chelating groups attached to the nitrogen atoms as potential ligands for asymmetric catalysis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F00%3A00006649" target="_blank" >RIV/00216208:11310/00:00006649 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388955:_____/00:54010187

  • Result on the web

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis of C-2-symmetrical [1,1 '-binaphthalene]-2,2 '-diamines with additional chelating groups attached to the nitrogen atoms as potential ligands for asymmetric catalysis

  • Original language description

    Reductive amination of 2-hydroxybenzaldehyde, using a combination of NaBH4 and (R)-[1,1'-binaphthalene]-2,2'-diamine, served as the key step in the synthesis of the potentially tetradentate ligands.

  • 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

    <a href="/en/project/GA203%2F98%2F1185" target="_blank" >GA203/98/1185: Binaphtyl ligands with bulky and chelating groups in 2,22' - positions and their application for asymmetric synthesis</a><br>

  • Continuities

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2000

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Collection of Czechoslovak Chemical Communications

  • ISSN

    0010-0765

  • e-ISSN

  • Volume of the periodical

    65

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    CZ - CZECH REPUBLIC

  • Number of pages

    10

  • Pages from-to

  • UT code for WoS article

  • EID of the result in the Scopus database