Informacja

Drogi użytkowniku, aplikacja do prawidłowego działania wymaga obsługi JavaScript. Proszę włącz obsługę JavaScript w Twojej przeglądarce.

English (EN)·Polski (PL)·Yкраїнський (UK)
Przejdź do strony domowej biblioteki Centralna Biblioteka Wojskowa Link otwiera się w nowym oknie Logo biblioteki Prolib Integro - strona głównaCentralna Biblioteka Wojskowa

Wyszukujesz frazę "Kolodziejska, A." wg kryterium: Autor

  Lista filtrów
Wyrównaj
Wyświetlanie 1-15 z 30
Tytuł:
Prosta metoda izolacji limfocytów z krwi obwodowej człowieka
Simple method of isolation of lymphocytes from human peripheral blood
Autorzy:
Bergiel, A.
Kołodziejska, B.
Powiązania:
https://bibliotekanauki.pl/articles/2189244.pdf
Data publikacji:
1975
Wydawca:
Polskie Towarzystwo Diagnostyki Laboratoryjnej
Źródło:
Diagnostyka Laboratoryjna; 1975, 11, 4; 333-336
0867-4043
Pojawia się w:
Diagnostyka Laboratoryjna
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Proteolytic activity of the viscera and partial purification of acid proteases of squid Illex argentinus hepatopancreas
Proteolityczna aktywnosc wnetrznosci i czesciowe oczyszczenie kwasnych proteaz z watrobo-trzustki kalmarow Illex argentinus
Autorzy:
Kolodziejska, I.
Mazurek, A.
Powiązania:
https://bibliotekanauki.pl/articles/1372840.pdf
Data publikacji:
1995
Wydawca:
Instytut Rozrodu Zwierząt i Badań Żywności Polskiej Akademii Nauk w Olsztynie
Tematy:
bialko
zywnosc
homogenaty
enzymy
stabilnosc
mrozenie
aktywnosc proteolityczna
kalmary
Illex argentinus
autoliza
autolizaty
utrwalanie zywnosci
watrobotrzustka
Opis:
The squid hepatopancreas, containing 20-60% lipids, is not suitable on board vessel for producing fodder meal and is often discarded, although it constitutes the major part of the viscera and is a rich source of proteolytic enzymes. The proteolytic activity against hemoglobin at pH 3.0 of the extract of the he pato pan ere a s of frozen stored squid, calculated per mg of protein, is about 20 times higher than that of the extract of the rest of the viscera. Due to incubation of the homogenate at pH 3.0 at 30 and 40°C in 2 days a clear watery phase was formed, well separated from the oily fraction containing floating solid particles of the autolysate. In 2 days about 35 and 50% of the protein was hydrolysed at 20°C and 30-40°C, respectively, to degradation products not precipitated by TCA. The proteolytic activity of the autolyzed homogenate after 2 days at pH 3.0 is about 80 % of that of the original homogenate. Incubation at 40°C at pH 3.0 decreased the activity after 6 days by about 50%. In the autolysate of squid hepatopancreas the proteolytic activity at pH 3.0 in the absence of reducing compounds was almost totally due to aspartic proteases. In the presence of dithiothreitol the activity increased by about 50%, but the increase was only partly due to the presence of thiol proteases.
Zbadano aktywność proteolityczną ekstraktów enzymów z wnętrzności mrożonych kalmarów Illex argentinus wobec hemoglobiny przy pH 3 oraz określono wpływ temperatury i czasu inkubacji na stabilność enzymów i autolizę białek homogenatu z wątrobo-trzustki. Proteolityczna aktywność przy pH 3 ekstraktu enzymów z wątrobo-trzustki kalmarów jest w przeliczeniu na 1 mg białek około 20 razy większa niż aktywność ekstraktów z pozostałych wnętrzności. Po dwóch dniach inkubacji homogenatu z wątrobo-trzustki w temperaturze 20°C i 30—40°C hydrolizuje odpowiednio około 35% i 50% białek. Proteolityczna aktywność w zautolizowanym homogenacie obniża się w tych warunkach o około 20%. Aktywność proteolityczna w autolizacie wykazywana przy pH 3 w nieobecności substancji redukujących pochodzi nieomal całkowicie od proteaz asparaginowych. Autoliza białek wątrobo-trzustki kalmarów jest prostą i tanią drogą uzyskiwania częściowo oczyszczonego preparatu enzymów proteolitycznych aktywnych w kwaśnym środowisku. Jednocześnie ułatwia ona oddzielenie lipidów i części stałych od klarownego autolizatu. Autolizat może stanowić półprodukt do otrzymywania preparatu enzymów proteolitycznych o większej czystości.
Źródło:
Polish Journal of Food and Nutrition Sciences; 1995, 04, 3; 63-70
1230-0322
2083-6007
Pojawia się w:
Polish Journal of Food and Nutrition Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Budowa, mechanizm działania i znaczenie peptydów natriuretycznych w diagnozowaniu chorób serca u psów
The structure, mechanism of action and function of natriuretic peptides in heart failure diagnostic in dogs
Autorzy:
Kolodziejska, A.
Kander, M.
Depta, A.
Szweda, M.
Powiązania:
https://bibliotekanauki.pl/articles/861524.pdf
Data publikacji:
2010
Wydawca:
Krajowa Izba Lekarsko-Weterynaryjna
Tematy:
peptydy natriuretyczne
przedsionkowy peptyd natriuretyczny
mozgowy peptyd natriuretyczny
budowa
mechanizm dzialania
psy
choroby serca
diagnostyka
diagnostyka laboratoryjna
stezenie peptydow natriuretycznych
Źródło:
Życie Weterynaryjne; 2010, 85, 10
0137-6810
Pojawia się w:
Życie Weterynaryjne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
A correlation between the Canine Inflammatory Bowel Disease Activity Index score and the histopathological evaluation of the small intestinal mucosa in canine inflammatory bowel disease
Autorzy:
Rychlik, A.
Nieradka, R.
Kander, M.
Nowicki, M.
Wdowiak, M.
Kolodziejska-Sawerska, A.
Powiązania:
https://bibliotekanauki.pl/articles/31320.pdf
Data publikacji:
2012
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Opis:
The aim of this study was to assess the degree of correlation between the intensity of clinical symptoms and the macroscopic and histopathological evaluation of the small intestinal mucous membrane in dogs. The results point to a statistically significant correlation between the values of the CIBDAI index and the histopathological assessment of the duodenum mucous membrane in patients with minor and moderate intensity of the disease. The lowest correlation coefficient was obtained for the indicator comparing macroscopic and histopathological evaluations. A positive correlation between the CIBDAI score and the histopathological index offers a base for applying it in the monitoring and treatment of mild, moderate and severe cases of canine inflammatory bowel disease.
Źródło:
Polish Journal of Veterinary Sciences; 2012, 15, 2
1505-1773
Pojawia się w:
Polish Journal of Veterinary Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Asymetryczne przeniesienie wodoru do ketonów katalizowane związkami Rutenu(II) i Rodu(III)
Asymmetric transfer hydrogenation of ketones catalyzed by Ruthenium(II) and Rhodium(III) complexes
Autorzy:
Karczmarska-Wódzka, A.
Kołodziejska, R.
Studzińska, R.
Wróblewski, M.
Powiązania:
https://bibliotekanauki.pl/articles/172550.pdf
Data publikacji:
2012
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
transfer wodoru asymetryczny
związki kompleksowe Ru(II) i Rh(III)
chiralne ligandy
prochiralne związki karbonylowe
asymmetric transfer hydrogenation
Ru(II) and Rh(III) complexes
chiral ligands
prochiral carbonyl compounds
Opis:
Asymmetric hydrogen transfer (ATH) is one of the methods of stereoselective reduction of prochiral carbonyl compounds (Scheme 6). Complexes of the platinum group metals (Noyori catalysts) are the most common catalysts for AT H reactions. The specific structure of the Noyori catalyst allows to activate two hydrogen atoms. These atoms are transferred from donor to acceptor in the form of hydride ion and proton (Scheme 1). Depending on the used catalyst the transfer hydrogenation of ketons can proceed by direct and indirect transfer mechanism. The direct hydride transfer from a donor to an acceptor proceeds via a six-membered transition state (3) (Scheme 2). The indirect hydride transfer proceeds through the formation of an intermediate metal hydride. A monohydride (HLnMH) and or a dihydride (LnMH2) can be formed depending on the catalyst that is used (Scheme 3). In the monohydride route, the reduction proceeds in the inner sphere of the metal (four-membered transition state (4)) or in the outer sphere of the metal (six-membered transition state (5)) (Scheme 4). The proposed reduction of carbonyl compounds in the AT H reaction by Noyori catalysts uses the mechanism of the hydride ion and proton transfer from the donor to the catalyst and the formation of the monohydride. In the indirect transfer hydrogenation the hydride ion and proton are transferred from the monohydride to the acceptor (Scheme 5, 7). AT H reactions that lead to chiral alcohols are conducted in organic solvents or in water. Hydrogen donors most often used in organic solvent reactions are propan-2-ol or an azeotropic mixture of formic acid and triethylamine (Tab. 1, 6). Sodium formate is usually used as hydrogen donor in the reactions conducted in water. Yield and enantioselectivity of the reaction depend on many factors the most important of which are: the structure of a substrate, hydrogen donor and solvent that were used, the reaction time, substrate concentration, and the S/C ratio [2]. In the case of asymmetric reduction conducted in water the solvent pH is also of great importance [3, 7, 8]. An optimal pH range depends on the type of a catalyst [7, 8]. AT H reactions conducted in water are distinguished by a shorter reaction time and higher enantioselectivity than the reactions conducted in organic solvents. In addition, catalysts used in the AT H reactions are more stable in water allowing reuse of the catalyst without loss of its activity. This paper presented examples of the use of specific catalysts in asymmetric reactions of hydrogen transfer. In particular, I drew attention to the reactions running in the aquatic environment due to the above-mentioned advantages of this solvent. The authors focused specifically on bifunctional catalysts based on Ru(II) and Rh(III) on the account of wide usage of the catalysts of that type in AT H reactions in water and their good performance [8, 9, 15, 16, 17, 19, 20, 21, 22]. p-Cymene is the most common aromatic ligand in catalysts based on Ru(II) while in the case of catalysts with Rh(III) the most common is anionic pentamethylcyclopentadienyl ligand. In both cases the second most common ligands are diamines or amino alcohols (Scheme 8). There are better performance and enantioselectivity when diamines are used as ligands. Attempts to replace diamines and amino alcohols by Schiff bases (Scheme 13) in the catalysts containing Rh(III) proved poor results due to a very low enantioselectivity of conducted reactions (Tab. 7).
Źródło:
Wiadomości Chemiczne; 2012, 66, 3-4; 273-295
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Modulation of specific biochemical blood parameters by helminth infection in laboratory Beagle dogs
Autorzy:
Szweda, M.
Szarek, J.
Babinska, I.
Sokol, R.
Ras-Norynska, M.
Kolodziejska-Sawerska, A.
Mecik-Kronenberg, T.
Powiązania:
https://bibliotekanauki.pl/articles/31110.pdf
Data publikacji:
2012
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Opis:
The objective of this study was to examine the independent effect of helminths infection on biochemical blood parameters in Beagles intended for laboratory use which may contribute to a change of experimental results. As a result of research, the authors confirmed the negative effect of helminth invasion on the metabolism of the liver and kidney in laboratory dogs. Stool samples from thirty Beagle puppies were examined for parasites before the puppies were moved to the animal facility, and all were dewormed with Vetminth paste on the day they were moved. Stool examination was performed three more times and animals were given Drontal Plus flavor (Bayer) and Baycox 5% (Bayer). A fourth parasitological examination revealed no intestinal parasites in the feces. Three blood biochemical tests were performed. Experimental results clearly indicate the significant impact of intestinal parasites in dogs used in experiments.
Źródło:
Polish Journal of Veterinary Sciences; 2012, 15, 2
1505-1773
Pojawia się w:
Polish Journal of Veterinary Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Uses of tree saps in northern and eastern parts of Europe
Autorzy:
Svanberg, I.
Soukand, R.
Luczaj, L.
Kalle, R.
Zyryanova, O.
Denes, A.
Papp, N.
Nedelcheva, A.
Seskauskaite, D.
Kolodziejska-Degorska, I.
Kolosova, V.
Powiązania:
https://bibliotekanauki.pl/articles/57637.pdf
Data publikacji:
2012
Wydawca:
Polskie Towarzystwo Botaniczne
Źródło:
Acta Societatis Botanicorum Poloniae; 2012, 81, 4
0001-6977
2083-9480
Pojawia się w:
Acta Societatis Botanicorum Poloniae
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Biomarkers in canine inflammatory bowel disease diagnostics
Autorzy:
Wdowiak, M.
Rychlik, A.
Kolodziejska-Sawerska, A.
Powiązania:
https://bibliotekanauki.pl/articles/31118.pdf
Data publikacji:
2013
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Opis:
Canine inflammatory bowel disease (IBD) is a heterogeneous group of chronic gastrointestinal disorders. The etiology, similar to human IBD, remains unknown. Canine IBD is diagnosed by exclusion, which is a long, time and money-consuming process due to the need of elimination of other diseases presenting with similar symptoms. Therefore, a search for a specific and sensitive marker is needed to overcome these difficulties. The article is divided into 3 sections presenting up-to-date information about laboratory markers, immunohistochemical markers and changes in the neurochemical coding of the enteric nervous system, concentrating on their usefulness and future applications. Data concerning laboratory and immunohistochemical markers is based mainly on canine IBD, while the neuroimmunohistochemistry section presents knowledge from human IBD due to the lack of such studies in veterinary medicine.
Źródło:
Polish Journal of Veterinary Sciences; 2013, 16, 3
1505-1773
Pojawia się w:
Polish Journal of Veterinary Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Cytokines in canine inflammatory bowel disease
Autorzy:
Kolodziejska-Sawerska, A.
Rychlik, A.
Depta, A.
Wdowiak, M.
Nowicki, M.
Kander, M.
Powiązania:
https://bibliotekanauki.pl/articles/32308.pdf
Data publikacji:
2013
Wydawca:
Polska Akademia Nauk. Czytelnia Czasopism PAN
Opis:
Canine inflammatory bowel disease is a group of chronic enteropathies characterized by persistent or recurring gastric symptoms with an unknown etiology which are related to histopathological changes in the mucosa of the small and large bowel in the form of cellular infiltration in the mucosal lamina propria. Recent years have witnessed a growing number of investigations into the role of the immune system and, in particular, cytokines in the development of IBD. In this article, the expression of pro-inflammatory (IL-1, IL-2, IL-5, IL-6, IL-12, IL-18, IFN-γ, TNF-α) and anti-inflammatory cytokines (IL-4, IL-10) was compared in canine patients with IBD based on clinical presentation, breed, lamina propria cell infiltrate and histopathological grade. Only selected studies confirmed higher mRNA expression levels of cytokines IL-2, IL-4, IL-5, IL-12p40, IFN-γ, TNF-α and TGF-β in dogs with IBD in comparison with healthy subjects. GSD were strongly represented in most study populations. Dogs with LPE were characterized by elevated levels of IL-1α, IL-1β, IL-2, IL-5, IL-6, IL-12, TNF-α, TGF-β. The present studies of canine patients with LPC revealed the mRNA expression of cytokines IL-1β, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12p35, IL-12p40, IFN-γ, TNF-α, TGF-β. In the reviewed studies, the progression of IBD was not accompanied by changes in the mRNA expression of IL-1α, IL-1β, IL-2, IL-4, IL-5, IL-6, IL-10, IL-12, IL-18, TNF-α, IFN-γ or TGF-β.
Źródło:
Polish Journal of Veterinary Sciences; 2013, 16, 1
1505-1773
Pojawia się w:
Polish Journal of Veterinary Sciences
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Enancjoselektywna enzymatyczna desymetryzacja katalizowana lipazami. Część 1, Związki prochiralne
Enantioselectve enzymatic desymmetrization catalyzed in the presence of lipase. Part 1, Prochiral compounds
Autorzy:
Kołodziejska, R.
Karczmarska-Wódzka, A.
Tafelska-Kaczmarek, A.
Studzińska, R.
Dramiński, M.
Powiązania:
https://bibliotekanauki.pl/articles/171684.pdf
Data publikacji:
2013
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
związki prochiralne
desymetryzacja
transestryfikacja
hydroliza
lipazy
prochiral compounds
desymmetrization
transesterification
hydrolysis
lipase
Opis:
In the enzymatic asymmetric synthesis, the enzyme allows the desymmetrization of achiral compounds resulting in chiral compounds of high optical purity. Therefore, this type of biotransformation is known as enantioselective enzymatic desymmetrization (EED) [1–11]. This method is related to the generation of an asymmetry (loss of symmetry elements) in prochiral molecules (most often an sp3 or sp2 hybridized carbon atom), in meso synthones, and centrosymmetric compounds. An achiral center of the tetrahedral system is defined as a prochiral one if it becomes chiral as a result of one of the two substituents replacement which, when separated from the particles, are indistinguishable (Scheme 1, 2) [1–4, 9, 12]. Asymmetric synthesis is enantioselective when one of the enantiotopic groups or faces of an optically inactive compound is biotransformed faster than the other (Scheme 3–5) [1, 10, 11, 13–15]. Lipases are enzymes of highest importance in stereoselective organic synthesis, mainly due to their exceptionally broad substrate tolerance, stability, activity in unphysiological systems, and relatively low price [9, 14]. The mechanism of enzymatic hydrolysis catalysed by hydrolases is similar to that observed in the chemical hydrolysis with the use of base. The selectivity of enzymatic catalysis depends on the substrate orientation in the enzyme active site (Scheme 6, 7) [25–29]. Lipases were successfully used for the desymmetrization of different prochiral diesters, alcohols and amines. Most lipases preferentially convert the same prochiral groups in the above mentioned types of reaction. This allows the preparation of the both enantiomers of the product in high chemical and optical yield (Scheme 9–13) [9, 13, 32–56].
Źródło:
Wiadomości Chemiczne; 2013, 67, 7-8; 751-772
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Enancjoselektywna enzymatyczna desymetryzacja katalizowana lipazami. Część II, Optymalizacja warunków reakcji. Związki mezo
Enantioselectve enzymatic desymmetrization catalyzed in the presence of lipase. Part II, Optymalization of reaction conditions. Meso compounds
Autorzy:
Karczmarska-Wódzka, A.
Kołodziejska, R.
Tafelska-Kaczmarek, A.
Przybyła, T.
Dramiński, M.
Powiązania:
https://bibliotekanauki.pl/articles/172192.pdf
Data publikacji:
2013
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
związki mezo
desymetryzacja
transestryfikacja
hydroliza
lipaza
meso compounds
desymmetrization
transesterification
hydrolysis
lipase
Opis:
In the enzymatic asymmetric synthesis, the enzyme allows the desymmetrization of achiral compounds resulting in chiral compounds of high optical purity. Meso compounds (bearing a plane of symmetry) are very important group of compounds used in EEDs (Scheme 1) [1–4]. Similarly to prochiral compounds, selective acylation or hydrolysis of meso substrates leads to optically active products. Most lipases preferentially convert the same enantiomers in the above mentioned types of reaction. This allows the preparation of the both enantiomers of the product in high chemical and optical yield (Scheme 3–20) [35–58]. An effective enzymatic catalysis should be performed under conditions optimal for a biocatalyst performance. Hence, it is essential to select an appropriate reaction medium, the pH, and temperature [6–34]. Optimization of the reaction conditions in terms of an appropriate solvent selection is effective and most frequently the simplest way to modify the enzyme selectivity. One of the most important criteria for the solvent selection is its nature [25]. The enzyme selectivity is conditioned by its conformational rigidity, which increases in more hydrophobic medium (typical hydrophobic solvents, scCO2). A hydrophobic solvent decreases biocatalyst lability, which does not allow the connection between the structurally mismatched substrate and the active side of an enzyme [10, 26–31]. Ionic liquids are a separate group of solvents which, despite their high hydrophobicity (logP << 0) and polarity, can constitute an ideal medium for the biotransformation reactions [18–23].
Źródło:
Wiadomości Chemiczne; 2013, 67, 9-10; 819-841
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Prolina – pospolity aminokwas wyjątkowy katalizator. Część I, Biosynteza proliny. Wewnątrzcząsteczkowa kondensacja aldolowa
Proline as a common amino acid and an exceptional catalyst. Part I, Proline biosynthesis. Intramolecular aldol reaction
Autorzy:
Wróblewski, M.
Kołodziejska, R.
Studzińska, R.
Karczmarska-Wódzka, A.
Dramiński, M.
Powiązania:
https://bibliotekanauki.pl/articles/172473.pdf
Data publikacji:
2013
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
biosynteza proliny
mechanizm kondensacji aldolowej
wewnątrzcząsteczkowa reakcja aldolowa
proline biosynthesis
mechanism of aldol reaction
intramolecular aldol reaction
Opis:
In asymmetric synthesis of organic compounds more effective solutions are being looked for which will result in higher yield(s) of product(s) and their high enantioselectivity [1]. One of such solutions is an use of a multilevel and cheap catalyst. Proline used as a catalyst is a substance of natural origin which was synthetically obtained by Willstätter who was carrying out research on hygric acid (Scheme 1) [10]. The cells of many organisms have a suitable enzymatic system essential for proline biosynthesis [15]. So far, three proline biosynthesis pathways have been described: from glutamate (Scheme 3 and 4), ornithine (Scheme 5 and 6), and arginine (Scheme 7) [16–28]. Proline which is obtained as a result of biosynthesis or supplementation is a substrate for many proteins. Characteristic and significant content (about 23%) of this amino acid was observed in collage. In cells proline can play an important role of osmoregulator [31–35] – a protective substance regulating the activity of such enzymes as catalase and peroxidase [36]. Proline as a secondary amine shows exceptional nucleophilicity facilitating imine and enamine formation. Used as a catalyst in aldol reaction makes with substrates like imine or enamine transition state imitating the activity of naturally occurring enzymes for this type of reaction, that is aldolases. In their research Hajos and Parrish, and Eder, Sauer and Wiechert used proline in intramolecular aldol reaction obtaining proper enones (Scheme 9) [60–62]. The process of intramolecular aldol reaction was used for a separation of racemic mixture of diketones (Scheme 10) [63, 64], cyclization of ortho-substituted aromatic aldehydes and ketones (Scheme 11) [65], synthesis of cyclic diketones (Scheme 13) [68] and domino reaction to obtain substituted cyclohexanones from beta-diketones and unsaturated ketones (Scheme 14) [69].
Źródło:
Wiadomości Chemiczne; 2013, 67, 9-10; 801-818
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Prolina – pospolity aminokwas wyjątkowy katalizator. Część II, Międzycząsteczkowa kondensacja aldolowa
Proline as a common amino acid and an exceptional catalyst. Part II, Intermolecular aldol reaction
Autorzy:
Kołodziejska, R.
Wróblewski, M.
Karczmarska-Wódzka, A.
Studzińska, R.
Dramiński, M.
Powiązania:
https://bibliotekanauki.pl/articles/171560.pdf
Data publikacji:
2013
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
międzycząsteczkowa reakcja aldolowa donor
akceptor
prolina
anti-aldole
intermolecular aldol reaction
donor
acceptor
proline
anti-aldol
Opis:
Proline in organic synthesis is used as a small molecular organocatalyst. In a catalytic act proline, similarly to an enzyme, activates reagents, stabilizes transition state and influences an orientation of substrates [1–12]. Proline works as aldolase I (so called microaldolase I). In comparison with other amino acids it shows exceptional nucleophilicity which makes imines and enamines formation easier. In the intermolecular aldol reaction proline was used for the first time by List and co-workers (Scheme 1) [3, 9, 20]. Since then an immense progress has been observed in this field. Several aldolization reactions were performed in the presence of proline. Reactions of this type proceed between the donor (nucleophile) and the acceptor (electrophile). In aldol reaction the donors can be both ketones and aldehydes which next are condensed with ketones and aldehydes acting as electrophiles (Scheme 2–18; Tab. 1–7) [21–72]. The presence of proline ensures not only high yield of homo- and heteroaldolization but mainly enables conducting enantio- and diastereoselective synthesis. Intermolecular proline-catalyzed aldol condensation proceeds according to enamine mechanism. Anti-aldols, which make a valuable source of intermediates in the synthesis of important biologically active compounds, are mainly obtained in this reaction [35–44, 54, 58, 62, 63, 68, 69, 71].
Źródło:
Wiadomości Chemiczne; 2013, 67, 11-12; 1027-1050
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Enancjoselektywna enzymatyczna desymetryzacja katalizowana oksydoreduktazami. Dehydrogenazy w reakcji redukcji. Część I
Enantioselective enzymatic desymmetrization catalyzed by oxidoreductases. Dehydrogenases in reduction reactions. Part I
Autorzy:
Kołodziejska, R.
Karczmarska-Wódzka, A.
Tafelska-Kaczmarek, A.
Studzińska, R.
Wróblewski, M.
Augustyńska, B.
Powiązania:
https://bibliotekanauki.pl/articles/171686.pdf
Data publikacji:
2014
Wydawca:
Polskie Towarzystwo Chemiczne
Tematy:
redukcja asymetryczna
dehydrogenaza alkoholowa
kofaktor
asymmetric reduction
alcohol dehydrogenase
cofactor
Opis:
Enzymes act as biocatalysts whether are also mediating in all anabolic and catabolic pathways, playing an extremely important role in the cells of all life forms. Catalytic potential of oxidoreductases is most commonly used in reduction reactions. Dehydrogenases and reductases catalyze the reversible desymmetrization reactions of meso and prochiral carbonyl compounds and alkenes. The oxidoreductase- catalyzed reactions require cofactors to initiate catalysis. In most cases, it is nicotinamide adenine dinucleotide (NADH) or its phosphorylated derivative (NADPH), which acts as a hydride donor. The necessity of employing expensive cofactors was, for the long time, one of the main limitations to the use of dehydrogenases. This problem was solved by developing a regeneration system of a cofactor in the reaction environment. Various systems are used for the cofactor recycling. In the case of a carbonyl compound reduction, an irreversible oxidation of formic acid to carbon dioxide is most frequently used. In this paper, selected examples of whole-cell and isolated enzymes applications in the carbonyl compound reduction are discussed. The application of baker’s yeast, microorganisms and dehydrogenases in enantioselective enzymatic desymmetrization (EED) of prochiral ketones leads to a broad spectrum of chiral alcohols used as intermediates in the syntheses of many pharmaceuticals and compounds presenting a potential biological activity.
Źródło:
Wiadomości Chemiczne; 2014, 68, 9-10; 763-782
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
Enancjoselektywna enzymatyczna desymetryzacja katalizowana oksydoreduktazami. Reakcje redukcji. Część 2
Enantioselective enzymatic desymmetrization catalyzed by oxidoreductases. Reduction reactions. Part 2
Autorzy:
Kołodziejska, R.
Karczmarska-Wódzka, A.
Tafelska-Kaczmarek, A.
Studzińska, R.
Wróblewski, M.
Augustyńska, B.
Powiązania:
https://bibliotekanauki.pl/articles/171910.pdf
Data publikacji:
2014
Wydawca:
Polskie Towarzystwo Chemiczne
Opis:
Biotransformation reactions of many organic compounds under the influence of enzymes take place with the high selectivity, rarely achieved by other methods. Ketoesters represent an extensive group of selectively bioreduced compounds. Chiral hydroxyesters and, subsequently, hydroxyacids are valuable intermediates in the syntheses of various biologically active compounds. Acyclic α- and β-ketoesters are transformed to the corresponding (R)- and (S)-hydroxyesters by using a specific dehydrogenases. The whole-cells enzymes, e.g. baker’s yeast, may exhibit a different catalytic activity depending on the substrate structure. Baker’s yeast enzymes selectively reduce the cyclic β-ketoesters providing mainly anti diastereomers due to the lack of rotation around the single α,β carbon-carbon bond. The enzymatic reduction of the esters, cyclopentanone, and cyclohexanone derivatives gave the optically active anti-alcohol enantiomers. The reductive EED of prochiral α-ketoesters, as well as β-ketoesters is an interesting transformation in organic chemistry due to the importance of the resulting chiral α-hydroxy acids and their derivatives used as building blocks. Baker’s yeast-catalyzed reduction of alkyl esters derived from pyruvate and benzoylformate allows the preparation of the (R)-alcohols. Polyketones can also be subjected to the reductive EED to give different compounds bearing the quaternary stereogenic centers which are broadly applied in asymmetric synthesis. In asymmetric synthesis, similarly to carbon-oxygen double bonds, carbon-carbon double bonds of prochiral alkanes can be reduced to obtain the optically active saturated compounds. The reduction of alkenes is catalyzed by both, the whole cells (microorganisms, plant cells) as well as isolated enzymes belonging to the oxydoreductases, so-called ene-reductases. The whole-cell catalysts are suitable, most frequently, for the preparative scale syntheses, but they are less chemoselective in comparison to the isolated reductases. In the case of polyfunctionalized alkenes, microorganisms can cause the additional side reaction reducing the desired product yield.
Źródło:
Wiadomości Chemiczne; 2014, 68, 11-12; 1009-1030
0043-5104
2300-0295
Pojawia się w:
Wiadomości Chemiczne
Dostawca treści:
Biblioteka Nauki
Artykuł
Wyświetlanie 1-15 z 30

Ta witryna wykorzystuje pliki cookies do przechowywania informacji na Twoim komputerze. Pliki cookies stosujemy w celu świadczenia usług na najwyższym poziomie, w tym w sposób dostosowany do indywidualnych potrzeb. Korzystanie z witryny bez zmiany ustawień dotyczących cookies oznacza, że będą one zamieszczane w Twoim komputerze. W każdym momencie możesz dokonać zmiany ustawień dotyczących cookies