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Mendeleev Communications, 2003, Volume 13, Issue 3, Pages 153–154
DOI: https://doi.org/10.1070/MC2003v013n03ABEH001760
(Mi mendc4000)
 

This article is cited in 2 scientific papers (total in 2 papers)

A ‘substrate-divergent’ approach to chiral cyclopentanes and cyclohexanes from a common precursor based on levoglucosan

R. V. Bikbulatov, F. A. Akbutina, L. V. Spirikhin, M. S. Miftakhov

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation
Full-text PDF (82 kB) Citations (2)
Abstract: Acyclic 1,3-dithianes 8 and 9 were transformed to cyclopentane derivative 12 and cyclohexane derivative 10, respectively, by treatment with BuLi.
Document Type: Article
Language: English


Citation: R. V. Bikbulatov, F. A. Akbutina, L. V. Spirikhin, M. S. Miftakhov, “A ‘substrate-divergent’ approach to chiral cyclopentanes and cyclohexanes from a common precursor based on levoglucosan”, Mendeleev Commun., 13:3 (2003), 153–154
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  • https://www.mathnet.ru/eng/mendc/v13/i3/p153
  • This publication is cited in the following 2 articles:
    1. N. A. Ivanova, Z. R. Valiullina, O. V. Shitikova, M. S. Miftakhov, “Unexpected transformation of methyl 3,6-anhydro-2,7-dideoxy-7-iodo-4,5-O-isopropylidene-D-allo-heptonate in the dehydroiodination reaction with 1,8-diazabicyclo[5.4.0]undec-7-ene”, Russ Chem Bull, 54:11 (2005), 2698  crossref
    2. Ruslan V. Bikbulatov, Fanuza A. Akbutina, Leonid V. Spirikhin, Mansur S. Miftakhov, “A “Substrate‐Divergent” Approach to Chiral Cyclopentanes and Cyclohexanes from a Common Precursor Based on Levoglucosan.”, ChemInform, 34:46 (2003)  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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