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A New Allenyloxime Synthon in Heterocyclizations Leading to Stable Cyclic Nitrones

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F08%3A00051051" target="_blank" >RIV/00216224:14310/08:00051051 - isvavai.cz</a>

  • Result on the web

    <a href="http://www.chemicke-listy.cz/docs/full/2008_11_1021-1083.pdf" target="_blank" >http://www.chemicke-listy.cz/docs/full/2008_11_1021-1083.pdf</a>

  • DOI - Digital Object Identifier

Alternative languages

  • Result language

    angličtina

  • Original language name

    A New Allenyloxime Synthon in Heterocyclizations Leading to Stable Cyclic Nitrones

  • Original language description

    A variety of conditions including reductive and/or basic reagents in aqueous or alcoholic solution was applied to 2,2-dimethylpenta-3,4-dienal oxime. Formation of various five-membered heterocycles with excellent chemical selectivity was observed. Most of the reactions yielded cyclic nitrones with stable dipolar structure and unique functionalities present. All products of cyclization were isolated and fully characterized.

  • Czech name

  • Czech description

Classification

  • Type

    O - Miscellaneous

  • CEP classification

    CC - Organic chemistry

  • OECD FORD branch

Result continuities

  • Project

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2008

  • Confidentiality

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