Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Yuliya A. Khalilova"'
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
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:
Russian Journal of Organic Chemistry. 55:1088-1092
The addition of lithium enolates and TMS ethers of cyclohexanone and cyclododecanone to levoglucosenone in the presence of Lewis acids was studied. It was established that the optimal way to obtain of Michael adducts involves the reaction levoglucose
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::037acd282029530be1663be6cd73ecc7
https://doi.org/10.1134/s1070428019080050
https://doi.org/10.1134/s1070428019080050
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
Autor:
Shamil M. Salikhov, Farid A. Valeev, Yuliya S. Galimova, Yuliya A. Khalilova, Liliya Kh. Faizullina
Publikováno v:
Mendeleev Communications. 28:482-484
Action of bases on levoglucosenone-derived 6-oxononan-9-olide and 7-oxodecan-10-olide causes the transannular reaction of the aldol type affording stable 2-acylcyclopent-1-en-1-ol and 2-acylcyclohex-1-en-1-ol, respectively. The lower homologue, 5-oxo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ffdcff6cc034367305246ea1943c3c57
https://doi.org/10.1016/j.mencom.2018.09.009
https://doi.org/10.1016/j.mencom.2018.09.009