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Base-Mediated Intramolecular C- and N-Arylation of N,N-Disubstituted 2-Nitrobenzenesulfonamides: Advanced Intermediates for the Synthesis of Diverse Nitrogenous Heterocycles

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61989592%3A15310%2F14%3A33151969" target="_blank" >RIV/61989592:15310/14:33151969 - isvavai.cz</a>

  • Alternative codes found

    RIV/61989592:15110/14:33151969

  • Result on the web

    <a href="http://pubs.acs.org/doi/pdf/10.1021/co5000739" target="_blank" >http://pubs.acs.org/doi/pdf/10.1021/co5000739</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1021/co5000739" target="_blank" >10.1021/co5000739</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Base-Mediated Intramolecular C- and N-Arylation of N,N-Disubstituted 2-Nitrobenzenesulfonamides: Advanced Intermediates for the Synthesis of Diverse Nitrogenous Heterocycles

  • Original language description

    Structural and electronic features that facilitate and direct the intramolecular C- and N-arylation of 2-alkyl-2-{[N-(benzyl)-2-nitrophenyl]sulfonamido}acetic acid esters and amides were examined. The substitution pattern and amino acid carboxy-terminalfunctionality determined the arylation position. C/N-arylated products represent advanced intermediates for combinatorial synthesis of diverse nitrogenous heterocycles, including indazoles, quinazolinones, quinoxalinones, and 3-amino-2-oxindoles.

  • 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

    O - Projekt operacniho programu

Others

  • Publication year

    2014

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    ACS Combinatorial Science

  • ISSN

    2156-8952

  • e-ISSN

  • Volume of the periodical

    16

  • Issue of the periodical within the volume

    9

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    6

  • Pages from-to

    500-505

  • UT code for WoS article

    000341410000008

  • EID of the result in the Scopus database