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Amide Bond Formation via Aerobic Photooxidative Coupling of Aldehydes with Amines Catalyzed by a Riboflavin Derivative

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60461373%3A22310%2F21%3A43923619" target="_blank" >RIV/60461373:22310/21:43923619 - isvavai.cz</a>

  • Alternative codes found

    RIV/60461373:22810/21:43923619

  • Result on the web

    <a href="https://pubs.acs.org/doi/abs/10.1021/acs.orglett.1c02391" target="_blank" >https://pubs.acs.org/doi/abs/10.1021/acs.orglett.1c02391</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/acs.orglett.1c02391" target="_blank" >10.1021/acs.orglett.1c02391</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Amide Bond Formation via Aerobic Photooxidative Coupling of Aldehydes with Amines Catalyzed by a Riboflavin Derivative

  • Original language description

    We report an effective, operationally simple, and environmentally friendly system for the synthesis of tertiary amides by the oxidative coupling of aromatic or aliphatic aldehydes with amines mediated by riboflavin tetraacetate (RFTA), an inexpensive organic photocatalyst, and visible light using oxygen as the sole oxidant. The method is based on the oxidative power of an excited flavin catalyst and the relatively low oxidation potential of the hemiaminal formed by amine to aldehyde addition. © 2021 American Chemical Society.

  • 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/GA18-15175S" target="_blank" >GA18-15175S: Oxidative photocatalytic systems with flavinium salts for direct C-H functionalizations</a><br>

  • Continuities

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

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Organic Letters

  • ISSN

    1523-7060

  • e-ISSN

  • Volume of the periodical

    23

  • Issue of the periodical within the volume

    17

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

    6825-6830

  • UT code for WoS article

    000693633500043

  • EID of the result in the Scopus database

    2-s2.0-85114424652