Synthesis of uvarindole A View Full Text


Ontology type: schema:ScholarlyArticle     


Article Info

DATE

2014-11

AUTHORS

V. A. Osyanin, D. D. Borisov, D. V. Osipov, Yu. N. Klimochkin

ABSTRACT

Procedure was developed for the synthesis of an alkaloid of indole series uvarindole A. The key step of the synthesis is a successive indole alkylation with salicylic alcohol catalyzed with ZnCl2. The presumed intermediates are o-hydroxybenzyl carbocation and o-quinone methide.

PAGES

1590-1593

References to SciGraph publications

  • 2011-01. Reactions of indoles with 2- and 4-hydroxybenzyl alcohols in RUSSIAN JOURNAL OF GENERAL CHEMISTRY
  • 2011-11. 2-(2-hydroxyphenyl)-2-adamantanol in Ritter reaction in RUSSIAN JOURNAL OF ORGANIC CHEMISTRY
  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1134/s1070428014110098

    DOI

    http://dx.doi.org/10.1134/s1070428014110098

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1004008438


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