Образец цитирования:
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
Образцы ссылок на эту страницу:
https://www.mathnet.ru/rus/mendc2377
https://www.mathnet.ru/rus/mendc/v25/i4/p271
Эта публикация цитируется в следующих 10 статьяx:
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
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
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
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
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
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
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
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
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
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