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Applications of Bolm's Ligand in Enantioselective Synthesis

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F20%3A10414565" target="_blank" >RIV/00216208:11310/20:10414565 - isvavai.cz</a>

  • Result on the web

    <a href="https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Bi.p-3y2E-" target="_blank" >https://verso.is.cuni.cz/pub/verso.fpl?fname=obd_publikace_handle&handle=Bi.p-3y2E-</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.3390/molecules25040958" target="_blank" >10.3390/molecules25040958</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Applications of Bolm's Ligand in Enantioselective Synthesis

  • Original language description

    One pathway for the preparation of enantiomerically pure compounds from prochiral substrates is the use of metal complex catalysis with chiral ligands. Compared to the other frequently used chiral ligands, chiral 2,2&apos;-bipyridines have been underexploited, despite the data indicating that such ligands have considerable potential in synthetic chemistry. One of those is the so-called Bolm&apos;s ligand, a compound possessing chiral alcohol moieties in the side chains attached to the 2,2&apos;-bipyridine scaffold. Various metal salts have been used in combination with Bolm&apos;s ligand as potent catalysts able to bring about enantioselective alkylations, allylations, conjugate additions, desymmetrization of meso-epoxides, aldol reactions, etc. This review aims to summarize Bolm&apos;s ligand applications in the area of enantioselective synthesis over the last three decades since its preparation.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10401 - Organic chemistry

Result continuities

  • Project

    <a href="/en/project/GA17-07707S" target="_blank" >GA17-07707S: Development of New Syntheses of Azaheterocycles</a><br>

  • Continuities

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

Others

  • Publication year

    2020

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Molecules

  • ISSN

    1420-3049

  • e-ISSN

  • Volume of the periodical

    25

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    CH - SWITZERLAND

  • Number of pages

    14

  • Pages from-to

    958

  • UT code for WoS article

    000522454500194

  • EID of the result in the Scopus database

    2-s2.0-85079837819