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Mendeleev Communications, 2021, Volume 31, Issue 2, Pages 251–253
DOI: https://doi.org/10.1016/j.mencom.2021.03.036
(Mi mendc896)
 

Communications

An unusual acetylene–allene rearrangement in iodomethylates of cotarnine acetylene derivatives

L. Yu. Ukhina, L. G. Kuz'minab, T. N. Gribanovaa, L. V. Belousovaa, E. N. Shepelenkoc, G. S. Borodkina, O. I. Dmitrievaa, V. A. Podshibyakina, N. V. Stankevicha

a Institute of Physical and Organic Chemistry, Southern Federal University, Rostov-on-Don, Russian Federation
b N.S. Kurnakov Institute of General and Inorganic Chemistry, Russian Academy of Sciences, Moscow, Russian Federation
c Southern Scientific Center of the Russian Academy of Sciences, Rostov-on-Don, Russian Federation
Abstract: N-Methylation of cotarnine–phenol propargyl ethers conjugates with MeI affords the corresponding quaternary ammonium derivatives with retained acetylenic moiety. 3-Hydroxyalk-1-yn-1-yl analogues in the course of such iodomethylation undergo isomerization into allenic derivatives which are transformed into acetylenic ones upon dissolution in DMSO.
Keywords: cotarnine acetylene derivatives, isoquinolinium compounds, iodomethylation, acetylene–allene rearrangement, X-ray, quantum-chemical calculations.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (3.7 Mb)


Citation: L. Yu. Ukhin, L. G. Kuz'mina, T. N. Gribanova, L. V. Belousova, E. N. Shepelenko, G. S. Borodkin, O. I. Dmitrieva, V. A. Podshibyakin, N. V. Stankevich, “An unusual acetylene–allene rearrangement in iodomethylates of cotarnine acetylene derivatives”, Mendeleev Commun., 31:2 (2021), 251–253
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