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Mendeleev Communications, 2015, Volume 25, Issue 4, Pages 271–272
DOI: https://doi.org/10.1016/j.mencom.2015.07.013
(Mi mendc2377)
 

This article is cited in 10 scientific papers (total in 10 papers)

Communications

Synthesis of chiral 2,3-cis-fused butan-4-olides from levoglucosenone–1,3-diene Diels–Alder adducts

A. N. Davydova, A. A. Pershin, B. T. Sharipov, F. A. Valeev

Ufa Institute of Chemistry, Ufa Federal Research Centre of the Russian Academy of Sciences, Ufa, Russian Federation
Abstract: Acid-catalyzed Baeyer–Villiger oxidation of levoglucosenone–1,3-diene Diels–Alder adducts affords chiral 2,3-cis-fused (2R,3S,4S)- 4-hydroxymethylbutan-4-olides.
Document Type: Article
Language: English
Supplementary materials:
Supplementary_data_1.pdf (1.9 Mb)


Citation: A. N. Davydova, A. A. Pershin, B. T. Sharipov, F. A. Valeev, “Synthesis of chiral 2,3-cis-fused butan-4-olides from levoglucosenone–1,3-diene Diels–Alder adducts”, Mendeleev Commun., 25:4 (2015), 271–272
Linking options:
  • https://www.mathnet.ru/eng/mendc2377
  • https://www.mathnet.ru/eng/mendc/v25/i4/p271
  • This publication is cited in the following 10 articles:
    1. Tingting Xu, Xin Gao, Yuanzhang Li, Changqu Lin, Peipei Ma, Zhongzhong Bai, Jun Zhou, Hongli Wu, Fei Cao, Ping Wei, “Characterization of isolated starch from Isatis indigotica Fort. root and anhydro-sugars preparation using its decoction residues”, Biomass Conv. Bioref., 14:14 (2024), 16075  crossref
    2. Brett Pollard, Xin Liu, Luke A. Connal, Martin G. Banwell, Michael G. Gardiner, Craig Hutton, “The synthesis and manipulation of certain Diels–Alder adducts of levoglucosenone and iso-levoglucosenone”, Aust. J. Chem., 76:11 (2023), 797  crossref
    3. L. Kh. Faizullina, Yu. S. Galimova, F. A. Valeev, “Baeyer–Villiger Oxidation of Diastereomeric Michael Adducts of Levoglucosenone into Dilactones”, Russ J Org Chem, 56:2 (2020), 197  crossref
    4. Sami Fadlallah, Aurélien A.M. Peru, Amandine L. Flourat, Florent Allais, “A straightforward access to functionalizable polymers through ring-opening metathesis polymerization of levoglucosenone-derived monomers”, European Polymer Journal, 138 (2020), 109980  crossref
    5. Martin G. Banwell, Xin Liu, Luke A. Connal, Michael G. Gardiner, “Synthesis of Functionally and Stereochemically Diverse Polymers via Ring-Opening Metathesis Polymerization of Derivatives of the Biomass-Derived Platform Molecule Levoglucosenone Produced at Industrial Scale”, Macromolecules, 53:13 (2020), 5308  crossref
    6. Janis Rizhikovs, Prans Brazdausks, Galina Dobele, Vilhelmine Jurkjane, Aigars Paze, Kristine Meile, Maris Puke, “Pretreated hemp shives: Possibilities of conversion into levoglucosan and levoglucosenone”, Industrial Crops and Products, 139 (2019), 111520  crossref
    7. Bulat T. Sharipov, Anna N. Davidova, Alena S. Ryabova, Nailya F. Galimzyanova, Farid A. Valeev, “Synthesis and fungicidal activity of methylsulfanylmethyl ether derivatives of levoglucosenone”, Chem Heterocycl Comp, 55:1 (2019), 31  crossref
    8. María B. Comba, Yi‐hsuan Tsai, Ariel M. Sarotti, María I. Mangione, Alejandra G. Suárez, Rolando A. Spanevello, “Levoglucosenone and Its New Applications: Valorization of Cellulose Residues”, Eur J Org Chem, 2018:5 (2018), 590  crossref
    9. B. T. Sharipov, A. A. Pershin, F. A. Valeev, “Synthesis of sarcodictyin A analogue containing 14-methyl group and C(12)=C(13) bond in ring A from levoglucosenone”, Mendeleev Commun., 27:2 (2017), 119–121  mathnet  crossref
    10. I. M. Biktagirov, L. Kh. Faizullina, Sh. M. Salikhov, F. Z. Galin, M. G. Safarov, F. A. Valeev, “Oxidation with CrO3·2Py of levoglucosenone and 1,3-dienes Diels-Alder adducts”, Russ J Org Chem, 52:5 (2016), 711  crossref
    Citing articles in Google Scholar: Russian citations, English citations
    Related articles in Google Scholar: Russian articles, English articles
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