Protonation, deuteration, and formylation of aceperidazylenes View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-07

AUTHORS

V. V. Mezheritskii, L. G. Minyaeva, N. I. Omelichkin, A. A. Milov, K. A. Lysenko, A. F. Smolyakov

ABSTRACT

1H-1,2-Diazaphenalene derivatives in which the pyridazine ring is ortho- and peri-fused to acenaphthene and acenaphthylene (1H-indeno[6,7,1-def]cinnolines) have been synthesized. It has been found that electrophilic attack on these compounds is directed at C6.

PAGES

1022-1027

References to SciGraph publications

  • 2006-02. Oxidative transformations of peridazines in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1134/s107042801407015x

    DOI

    http://dx.doi.org/10.1134/s107042801407015x

    DIMENSIONS

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