D. A. Kulagina, S. V. Sysolyatin, V. V. Malykhin, A. I. Kalashnikov, “Acylation of 2,6,8,12-tetraacetyl-2,4,6,8,10,12- hexaazatetracyclo[5.5.0.03,11.05,9]dodecane”, Mendeleev Commun., 26:2 (2016), 139

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Mendeleev Communications, 2016, Volume 26, Issue 2, Pages 139–140
DOI: https://doi.org/10.1016/j.mencom.2016.03.019 (Mi mendc2138)

This article is cited in 5 scientific papers (total in 5 papers)

Communications

Acylation of 2,6,8,12-tetraacetyl-2,4,6,8,10,12- hexaazatetracyclo[5.5.0.0^3,11.0^5,9]dodecane

D. A. Kulagina^a, S. V. Sysolyatin^ab, V. V. Malykhin^a, A. I. Kalashnikov^a

^a Institute for Problems of Chemical & Energetic Technologies, Siberian Branch of the Russian Academy of Sciences, Biysk, Russian Federation
^b Department of Chemistry, National Research Tomsk State University, Tomsk, Russian Federation

Full-text PDF (143 kB) Citations (5)

DOI: https://doi.org/10.1016/j.mencom.2016.03.019

Graphic abstract: Acylation of 2,6,8,12-tetraacetyl-2,4,6,8,10,12- hexaazatetracyclo[5.5.0.0<sup>3,11</sup>.0<sup>5,9</sup>]dodecane

Abstract: 4-Mono- and 4,10-diacyl derivatives of 2,6,8,12-tetraacetyl-2,4,6,8,10,12-hexaazatetracyclo[5.5.0.0^3,11.0^5,9]dodecane were obtained by its treatment with acid chlorides in boiling acetonitrile.

Bibliographic databases:

Document Type: Article

Language: English

Citation: D. A. Kulagina, S. V. Sysolyatin, V. V. Malykhin, A. I. Kalashnikov, “Acylation of 2,6,8,12-tetraacetyl-2,4,6,8,10,12- hexaazatetracyclo[5.5.0.0^3,11.0^5,9]dodecane”, Mendeleev Commun., 26:2 (2016), 139–140

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https://www.mathnet.ru/eng/mendc2138

https://www.mathnet.ru/eng/mendc/v26/i2/p139

This publication is cited in the following 5 articles:

Citing articles in Google Scholar: Russian citations, English citations
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