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Mendeleev Communications, 2016, Volume 26, Issue 1, Pages 66–68
DOI: https://doi.org/10.1016/j.mencom.2016.01.026
(Mi mendc2113)
 

This article is cited in 6 scientific papers (total in 6 papers)

Communications

Dill and parsley seed extracts in scale up synthesis of aminopolyalkoxybenzenes – beneficial synthons for fused nitrogen polyalkoxyheterocycles

I. B. Karmanovaa, S. I. Firganga, L. D. Konyushkina, V. N. Khrustalevbc, A. V. Ignatovd, L. A. Kuznetsovd, Yu. A. Pinchuka, I. A. Kozlovd, V. V. Semenova

a N.D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
b A.N. Nesmeyanov Institute of Organoelement Compounds of Russian Academy of Sciences, Moscow, Russian Federation
c Peoples Friendship University of Russia (RUDN University), Moscow, Russian Federation
d "Russkii Katalizator" CJSC, Nizhnii Novgorod, Russian Federation
Full-text PDF (694 kB) Citations (6)
Abstract: Ecologically friendly transformation of readily accessible plant allylpolyalkoxybenzenes to hardly available aminotetraalkoxybenzenes has been developed. The efficacy of hydrogenation stage is substantially increased by the application of highly porous ceramic block Pd-catalysts featuring a large surface area, low hydraulic resistance, significant thermal and mechanical stabililty, multiple cycling and easy regeneration.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (505.6 Kb)


Citation: I. B. Karmanova, S. I. Firgang, L. D. Konyushkin, V. N. Khrustalev, A. V. Ignatov, L. A. Kuznetsov, Yu. A. Pinchuk, I. A. Kozlov, V. V. Semenov, “Dill and parsley seed extracts in scale up synthesis of aminopolyalkoxybenzenes – beneficial synthons for fused nitrogen polyalkoxyheterocycles”, Mendeleev Commun., 26:1 (2016), 66–68
Linking options:
  • https://www.mathnet.ru/eng/mendc2113
  • https://www.mathnet.ru/eng/mendc/v26/i1/p66
  • This publication is cited in the following 6 articles:
    1. V. E. Kalugin, O. I. Adaeva, D. V. Demchuk, V. V. Semenov, “Synthesis of new tetraalkoxyquinolines from parsley and dill secondary metabolites”, Mendeleev Commun., 33:4 (2023), 481–483  mathnet  crossref
    2. R. Alan Aitken, Comprehensive Heterocyclic Chemistry IV, 2022, 724  crossref
    3. A. E. Varakutin, E. A. Muravsky, I. Yu. Shinkarev, V. N. Khrustalev, V. V. Semenov, “Hydrogenation of plant polyalkoxybenzene derivatives: convenient access to coenzyme Q0 analogues”, Mendeleev Commun., 30:5 (2020), 599–601  mathnet  crossref
    4. A. V. Ignatov, A. E. Varakutin, I. N. Solov'eva, I. B. Karmanova, I. A. Kozlov, M. N. Semenova, V. V. Semenov, “Efficient hydrogenation of benzaldoximes and Schiff bases on ceramic high-porosity palladium catalysts”, Russ Chem Bull, 67:8 (2018), 1394  crossref
    5. Ekaterina V. Zaryanova, Alexander A. Ignatov, Nataly A. Lozynskaya, “Synthesis and reactivity of new amide-substituted oxindole derivatives”, Tetrahedron, 73:49 (2017), 6887  crossref
    6. R. Alan Aitken, Progress in Heterocyclic Chemistry, 29, 2017, 337  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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