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Direct C-H sulfenylation of purines and deazapurines

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216208%3A11310%2F13%3A10159260" target="_blank" >RIV/00216208:11310/13:10159260 - isvavai.cz</a>

  • Alternative codes found

    RIV/61388963:_____/13:00398636

  • Result on the web

    <a href="http://dx.doi.org/10.1039/c3ob40881g" target="_blank" >http://dx.doi.org/10.1039/c3ob40881g</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1039/c3ob40881g" target="_blank" >10.1039/c3ob40881g</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Direct C-H sulfenylation of purines and deazapurines

  • Original language description

    A general method for Cu-catalyzed C-H sulfenylation of purines, 7-deaza- and 9-deazapurines with aryl- or alkyldisulfides has been developed. In purines, the reaction occurs at position 8, in 7-deazapurines at position 7 and in 9-deazapurines at position9, leading to new interesting arylsulfanyl derivatives of purine or deazapurine bases. The resulting 8-arylsulfanylpurines undergo Liebesking-Srogl coupling with arylstannanes or boronic acids, whereas the (arylsulfanyl)deazapurines are not reactive under these conditions.

  • 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/GAP207%2F12%2F0205" target="_blank" >GAP207/12/0205: Development of novel methodologies of C-H activations of purines, deazapurines, pyrimidines and related heterocycles</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

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

    Organic and Biomolecular Chemistry

  • ISSN

    1477-0520

  • e-ISSN

  • Volume of the periodical

    11

  • Issue of the periodical within the volume

    31

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    5

  • Pages from-to

    5189-5193

  • UT code for WoS article

    000322855300018

  • EID of the result in the Scopus database