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Mendeleev Communications, 2021, Volume 31, Issue 4, Pages 493–494
DOI: https://doi.org/10.1016/j.mencom.2021.07.018
(Mi mendc966)
 

This article is cited in 3 scientific papers (total in 3 papers)

Communications

Intramolecular aldol condensation of Michael adducts of levoglucosenone and cyclododecanone

L. Kh. Faizullina, Yu. A. Khalilova, F. A. Valeev

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation
Full-text PDF (171 kB) Citations (3)
Abstract: Base-promoted intramolecular aldol condensation of diastereomeric Michael adducts of levoglucosenone and cyclododecanone affords 12-hydroxy-14,20-dioxatetra-cyclo[9.6.1.112,17.113,16]icosan-18-one as a mixture of three diastereomers. The products thus obtained are promising for synthesizing 14-membered macrocyclic compounds, including cembranoids and their analogues.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.6 Mb)


Citation: L. Kh. Faizullina, Yu. A. Khalilova, F. A. Valeev, “Intramolecular aldol condensation of Michael adducts of levoglucosenone and cyclododecanone”, Mendeleev Commun., 31:4 (2021), 493–494
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  • This publication is cited in the following 3 articles:
    Citing articles in Google Scholar: Russian citations, English citations
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