Zobrazeno 1 - 10
of 147
pro vyhledávání: '"Pyrrolidin 2 one"'
Autor:
Yassine Riadi, Mohamed H. Geesi, Rachid Azzallou, Oussama Dehbi, Oussama Ouerghi, Ammar Elsanousi
Publikováno v:
Polycyclic Aromatic Compounds. 42:6868-6882
Autor:
Veerappan Jeyachandran
Publikováno v:
International Journal of Scientific Research in Science and Technology. :10-15
A new class of chiral pyrrolidinone was synthesized from (5S)-5-[(trityloxy)methyl] pyrrolidin-2-one (6) (Schemes 1 and 2). The synthetic design followed led to the insertion of various substituents at 1 and 5 of the pyrrolidinone moiety. Some of the
Autor:
Natalja Orlova, Sergey Belyakov, Marina Petrova, Helena Kazoka, Vladislavs Baskevics, Ruslan Muhamadejev, Grigory Veinberg, Maxim Vorona
Publikováno v:
Chemistry of Heterocyclic Compounds. 56:997-1009
The addition of malonates to trans-β-alkyl-β-nitrostyrenes in the presence of chiral Mg2+ bisoxazoline complex and Ni2+ and Co2+ bis((S,S)- or (R,R)-N,N′-dibenzylcyclohexane-1,2-diamine) complexes resulted in the formation of Michael adducts with
Publikováno v:
Journal of Research on the Lepidoptera. 51:362-373
Publikováno v:
Acta Scientifci Nutritional Health. 4:30-33
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::44360c8ae5ba2876b73b7491cef1aac0
https://doi.org/10.31080/asnh.2020.04.utilization-of-a-pyrrolidin-one-based-nonselective-adrenoceptor-antagonist-for-metabolic-syndrome-(mets)-therapy-along-with-histamine-h-inverse-agonist-pitolistant-in-high-fat-diet-induced-obesity-in-mice-and-future-role
https://doi.org/10.31080/asnh.2020.04.utilization-of-a-pyrrolidin-one-based-nonselective-adrenoceptor-antagonist-for-metabolic-syndrome-(mets)-therapy-along-with-histamine-h-inverse-agonist-pitolistant-in-high-fat-diet-induced-obesity-in-mice-and-future-role
Publikováno v:
Current Microwave Chemistry. 5:97-103
Publikováno v:
Rasayan Journal of Chemistry. 14:82-87
Autor:
Alina Ghinet, Christophe Furman, Benoît Rigo, Anca-Elena Dascalu, Antoine Fayeulle, Emmanuelle Lipka, Muriel Billamboz
Publikováno v:
Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, 2020, 30 (13), pp.127220. ⟨10.1016/j.bmcl.2020.127220⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2020, 30 (13), pp.127220. ⟨10.1016/j.bmcl.2020.127220⟩
Bioorganic and Medicinal Chemistry Letters, 2020, 30 (13), pp.127220. ⟨10.1016/j.bmcl.2020.127220⟩
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2020, 30 (13), pp.127220. ⟨10.1016/j.bmcl.2020.127220⟩
International audience; Twenty-eight 5-pyrrolidine-2-ones decorated by hydrazine or acyl hydrazones groups have been designed, synthesized and evaluated as antifungal agents on a panel of twelve fungal strains and three non albicans candida yeasts sp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::644e7408e6592d09f72044a5da1ae583
https://hal.utc.fr/hal-02902219/document
https://hal.utc.fr/hal-02902219/document
Publikováno v:
International Letters of Chemistry, Physics and Astronomy. 79:17-28
A series of new spirooxindole derivatives were synthesized via 1,3 –dipolar cycloaddition. All the synthesized compounds were evaluated for antimicrobial activity. In antibacterial studies compound 4d demonstrated the most potent inhibitory activit
Publikováno v:
Synthetic Communications. 48:1324-1330
A facile regio and stereoselective synthesis of novel spiro[indolin-3,2′-pyrrolidin]-2-one’s have been accomplished through 1,3-dipolar cycloaddition of azomethine ylides generated in situ from the...