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Reaction of some 2-quinolone derivatives with phosphoryl chloride: Synthesis of novel phosphoric acid esters of 4-hydroxy-2-quinolone

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28110%2F13%3A43870018" target="_blank" >RIV/70883521:28110/13:43870018 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1002/jhet.1082" target="_blank" >http://dx.doi.org/10.1002/jhet.1082</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1002/jhet.1082" target="_blank" >10.1002/jhet.1082</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Reaction of some 2-quinolone derivatives with phosphoryl chloride: Synthesis of novel phosphoric acid esters of 4-hydroxy-2-quinolone

  • Original language description

    3-Chloroquinoline-2,4-diones do not react with phosphoryl chloride, however, 2,4-dichloroquinolines and/or 4-chloroquinolin-2-ones are formed in the presence of N,N-dimethylaniline. Along with these compounds, small quantities of novel dihydrogen phosphates of 4-hydroxyquinolin-2-ones were isolated. We outline a simple procedure that allows for the preparation of these compounds in moderate to good yields. All compounds were characterized by 1H and 13C NMR, IR, EI-MS, and ESI-MS spectroscopy, and in select cases by 31P NMR spectroscopy. Copyright 2013 HeteroCorporation.

  • 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%2F07%2F0320" target="_blank" >GA203/07/0320: Transformations of 3-hydroxy, 3-amino, and 3-thiocyanatoquinoline-2,4(1H,3H)-diones to novel heterocyclic systems</a><br>

  • Continuities

    Z - Vyzkumny zamer (s odkazem do CEZ)<br>S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2013

  • 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 heterocyclic chemistry

  • ISSN

    0022-152X

  • e-ISSN

  • Volume of the periodical

    50

  • Issue of the periodical within the volume

    SUPPL.1

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    11

  • Pages from-to

    "E100"-"E110"

  • UT code for WoS article

    000318428200015

  • EID of the result in the Scopus database