Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Liliya Kh. Faizullina"'
Autor:
Liliya Kh. Faizullina, Yuliya A. Khalilova, Liliya Sh. Karamysheva, Shamil M. Salikhov, Farid A. Valeev
Publikováno v:
Mendeleev Communications. 32:546-548
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb580b7e5b1d611f5e32b7ff677e1357
https://doi.org/10.1016/j.mencom.2022.07.037
https://doi.org/10.1016/j.mencom.2022.07.037
Autor:
A. V. Samorodov, Liliya Kh. Faizullina, Valentin Pavlov, Yuliya А. Khalilova, Farid А. Valeev
Publikováno v:
Chemistry of Heterocyclic Compounds. 57:966-969
A procedure for the preparation of an adduct of levoglucosenone and resorcinol was developed involving ultrasonic irradiation in the presence of K2CO3 and 18-crown-6 ether in toluene. In vitro anticoagulant and antiplatelet activity of the adduct was
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f09d86d6f5841fd42fcbc18031aac25d
https://doi.org/10.1007/s10593-021-03007-0
https://doi.org/10.1007/s10593-021-03007-0
Publikováno v:
Mendeleev Communications. 33:9-10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::21e3596190ca0377ec160f7ced74f621
https://doi.org/10.1016/j.mencom.2023.01.002
https://doi.org/10.1016/j.mencom.2023.01.002
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:1434-1439
Levoglucosenone reacted with α-ethoxycarbonyl- and α-nitrocyclododecanones, leading to the formation of diastereomeric Michael adducts in high yields. Methods were developed for the denitration of the respective nitroadducts by treatment with Raney
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e611ef9522369a0b1824e9062dbc43fd
https://doi.org/10.1007/s10593-020-02834-x
https://doi.org/10.1007/s10593-020-02834-x
Publikováno v:
Butlerov Communications. 62:20-25
Levoglucosenone has established itself as a good Michael acceptor and a powerful dienophile in Diels-Alder reactions, dipolar cycloaddition and in a number of other transformations. In the Diels-Alder reactions of levoglucosenone with 1,3-dienes, chi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fefd7a3e1cc45fe187befb323de3c24
https://doi.org/10.37952/roi-jbc-01/20-62-6-20
https://doi.org/10.37952/roi-jbc-01/20-62-6-20
Autor:
Liliya Kh. Faizullina, Yuliya S. Galimova, Yuliya A. Khalilova, Artur R. Tagirov, Shamil M. Salikhov, Farid A. Valeev
Publikováno v:
Mendeleev Communications. 32:632-633
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f48b7a1350bb7fcd032550ef6599a558
https://doi.org/10.1016/j.mencom.2022.09.021
https://doi.org/10.1016/j.mencom.2022.09.021
Publikováno v:
Chemistry of Heterocyclic Compounds. 55:612-618
Heating of solutions of the internal hemiketal, obtained by opening the 1,6-anhydro bridge in the Michael adduct of levoglucosenone and cyclohexanone, under reflux in THF or diglyme in the presence of NaH or Na, respectively, leads to the reduction o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c5d097a6cfa0838f74d755fd97b689ba
https://doi.org/10.1007/s10593-019-02506-5
https://doi.org/10.1007/s10593-019-02506-5
Publikováno v:
Mendeleev Communications. 31:493-494
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 thu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::914280bdf468b59878dc4dc6907557f9
https://doi.org/10.1016/j.mencom.2021.07.018
https://doi.org/10.1016/j.mencom.2021.07.018
Publikováno v:
Chemistry of Heterocyclic Compounds. 54:598-603
A synthetic route was developed consisting of 10 steps for the synthesis of ketodecanolide with native topology in 11% overall yield, starting from Michael adducts of levoglucosenone and cyclohexanone.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::017760a57109bd85bf75426bdfb7fcfa
https://doi.org/10.1007/s10593-018-2314-y
https://doi.org/10.1007/s10593-018-2314-y
Publikováno v:
Mendeleev Communications. 29:200-202
Diastereomerically pure levoglucosenone alcohol, synthesized from levoglucosenone, upon hydrogenation on Raney Ni or Pd/BaSO4 undergoes epimerization at C2 atom caused by formation of cyrene by-product and its subsequent non-specific reduction. A mic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4a914cad09fcc8731b297d4926c161c4
https://doi.org/10.1016/j.mencom.2019.03.029
https://doi.org/10.1016/j.mencom.2019.03.029