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Stereochemistry of the reduction of α-chloroketones with sodium borohydride-application to 3-chloroquinoline-2,4-diones: Dedicated to the memory of Professor Dr. Vojeslav Štěrba who died in September 2015 being nearly 93 years old

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F70883521%3A28110%2F16%3A43874516" target="_blank" >RIV/70883521:28110/16:43874516 - isvavai.cz</a>

  • Result on the web

    <a href="http://dx.doi.org/10.1016/j.tet.2016.05.087" target="_blank" >http://dx.doi.org/10.1016/j.tet.2016.05.087</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1016/j.tet.2016.05.087" target="_blank" >10.1016/j.tet.2016.05.087</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Stereochemistry of the reduction of α-chloroketones with sodium borohydride-application to 3-chloroquinoline-2,4-diones: Dedicated to the memory of Professor Dr. Vojeslav Štěrba who died in September 2015 being nearly 93 years old

  • Original language description

    3-Chloroquinoline-2,4-diones were reduced with sodium borohydride to give syn- and anti-chlorohydrins, the stereochemistry of which was established by NMR spectroscopy. Both stereoisomeric chlorohydrins were reacted with potassium carbonate in methanol. anti-Isomers afforded the corresponding epoxides or rearranged to 3-hydroxy-4-alkylquinolin-2-ones, whereas syn-isomers did not react. However, these isomers converted to 4-hydroxyquinolin-2-ones after standing for a long period of time in DMSO. After reaction with thionyl chloride, the syn-isomers yielded cis- and trans-3,4-dichloroquinolin-2-ones.

  • 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

  • Continuities

    S - Specificky vyzkum na vysokych skolach

Others

  • Publication year

    2016

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Tetrahedron

  • ISSN

    0040-4020

  • e-ISSN

  • Volume of the periodical

    72

  • Issue of the periodical within the volume

    30

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    8

  • Pages from-to

    4490-4497

  • UT code for WoS article

    000380073300002

  • EID of the result in the Scopus database

    2-s2.0-84976530940