Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Aneta Wroblewska"'
Autor:
Irena Bak-Sypien, Tomasz Pawlak, Piotr Paluch, Aneta Wroblewska, Rafał Dolot, Aleksandra Pawlowicz, Małgorzata Szczesio, Ewelina Wielgus, Sławomir Kaźmierski, Marcin Górecki, Roza Pawlowska, Arkadiusz Chworos, Marek J. Potrzebowski
Publikováno v:
Scientific Reports, Vol 14, Iss 1, Pp 1-18 (2024)
Abstract Cyclic tetrapeptides c(Pro-Phe-Pro-Phe) obtained by the mechanosynthetic method using a ball mill were isolated in a pure stereochemical form as a homochiral system (all L-amino acids, sample A) and as a heterochiral system with D configurat
Externí odkaz:
https://doaj.org/article/c063d4a0543840af82f2c1cd7682cbce
This book provides a detailed study of nonlinear partial differential equations satisfying certain nonstandard growth conditions which simultaneously extend polynomial, inhomogeneous and fully anisotropic growth. The common property of the many diffe
Publikováno v:
Journal of Fluorine Chemistry. 189:1-6
The 2-unsubstituted imidazole N-oxides with a 3,3,3-trifluoro-2-hydroxypropyl group at N(1) in the presence of acetic anhydride undergo cyclization via the intramolecular nucleophilic attack of the hydroxyl group onto C(2) of the imidazole ring to gi
Publikováno v:
Scopus-Elsevier
The 2-unsubstituted 1H-imidazole 3-oxides, considered as ‘nitrone-like’ azaheterocycles, are well known as versatile building blocks, useful for the preparation of more complex systems containing an imidazole moiety. Their applications in diverse
Publikováno v:
Asian Journal of Organic Chemistry. 4:770-777
Reactions of l-prolinol with aryl glyoxals lead to labile bicyclic 2-aryloyl-1,3-oxazolidines, which smoothly undergo isomerization in the presence of an acid via a cascade of reactions involving a 1,2-aryl shift. The products formed thereby were ide
Publikováno v:
Tetrahedron: Asymmetry. 26:505-509
The N-Boc-protected (S)-prolinamine reacts readily with formaldehyde and diverse α-hydroxyimino ketones to give imidazole N-oxides with an enantiomerically pure N-protected (pyrrolidin-2-yl)methyl substituent. Subsequent deprotection yields the corr
Publikováno v:
Tetrahedron: Asymmetry. 24:958-965
Starting with (S)-1-benzylprolinamine and α-hydroxyimino ketones, enantiomerically pure bisheterocyclic imidazole N-oxides bearing the (S)-configured N-benzyl(pyrrolidin-2-yl)methyl residue were prepared. These N-oxides reacted with 2,2,4,4-tetramet
Publikováno v:
ChemInform. 47
An intramolecular cyclization of enantiopure N(1)-(2-hydroxylpropyl)imidazole N-oxides, prepared by cyclocondensation of hydroxyethanols, formaldehyde, and α-ketoximes in the presence of acetic anhydride provides trifluoromethylated 2,3-dihydroimida
Publikováno v:
ChemInform. 47
The 2-unsubstituted 1H-imidazole 3-oxides, considered as ‘nitrone-like’ azaheterocycles, are well known as versatile building blocks, useful for the preparation of more complex systems containing an imidazole moiety. Their applications in diverse
Publikováno v:
ChemInform. 47
Optically active polyheterocycles containing pyrrolidine, imidazole, and 1,2,3-triazole units were obtained via a multistep synthesis with the [3+2] cycloaddition of Boc-protected (S)-(pyrrolidin-2-yl)methyl azide with 2-ethynylimidazoles in the pres