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Synthesis of new bipyridine N,N,-dioxides and their application in asymmetric allylation of benzaldehyde and aldol addition to acetophenone

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F68378271%3A_____%2F19%3A00518983" target="_blank" >RIV/68378271:_____/19:00518983 - isvavai.cz</a>

  • Alternative codes found

    RIV/00216208:11310/19:10393755

  • Result on the web

    <a href="https://doi.org/10.1007/s00706-018-2289-5" target="_blank" >https://doi.org/10.1007/s00706-018-2289-5</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1007/s00706-018-2289-5" target="_blank" >10.1007/s00706-018-2289-5</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Synthesis of new bipyridine N,N,-dioxides and their application in asymmetric allylation of benzaldehyde and aldol addition to acetophenone

  • Original language description

    Chiral pyridine N-oxides and bipyridine N,N´-dioxides are an important class of heteroaromatic compounds with interesting chemical properties. Polarization of the N–O bond results in their electron-donation activity and makes them rather strong Lewis bases, which are able to activate Lewis acids such as trichlorosilanes. Therefore, they can catalyze a number of various reactions such as allylation and crotylation of aldehydes, aldol reactions, ring-opening of epoxides, and cyanosilylation of ketones and imides. Due to the general high interest in the development of new Lewis basic chiral organocatalysts, synthetic approaches providing new chiral compounds possessing the pyridine N-oxide moiety are desirable.n

  • 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

    10302 - Condensed matter physics (including formerly solid state physics, supercond.)

Result continuities

  • Project

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

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2019

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Monatshefte fur Chemie

  • ISSN

    0026-9247

  • e-ISSN

  • Volume of the periodical

    150

  • Issue of the periodical within the volume

    1

  • Country of publishing house

    AT - AUSTRIA

  • Number of pages

    20

  • Pages from-to

    29-48

  • UT code for WoS article

    000454953600005

  • EID of the result in the Scopus database

    2-s2.0-85056640511