Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Stanisław Skóra"'
Autor:
Maja Sołtyka-Krajewska, Marcin Ziemniak, Anna Zawadzka-Kazimierczuk, Paulina Skrzypczyk, Ewelina Siwiak-Niedbalska, Anna Jaśkiewicz, Rafał Zieliński, Izabela Fokt, Stanisław Skóra, Wiktor Koźmiński, Krzysztof Woźniak, Waldemar Priebe, Beata Pająk-Tarnacka
Publikováno v:
Biomedicines, Vol 12, Iss 10, p 2240 (2024)
Background: One defining feature of various aggressive cancers, including glioblastoma multiforme (GBM), is glycolysis upregulation, making its inhibition a promising therapeutic approach. One promising compound is 2-deoxy-d-glucose (2-DG), a d-gluco
Externí odkaz:
https://doaj.org/article/6d606b7bd79e4c7ba8de139e5102bb5f
Autor:
Beata Pająk, Ewelina Siwiak-Niedbalska, Anna Jaśkiewicz, Maja Sołtyka, Rafał Zieliński, Tomasz Domoradzki, Izabela Fokt, Stanisław Skóra, Waldemar Priebe
Publikováno v:
Biomedicines, Vol 9, Iss 12, p 1749 (2021)
Over the last decade, we have seen tremendous progress in research on 2-deoxy-D-glucose (2-DG) and its analogs. Clinical trials of 2-DG have demonstrated the challenges of using 2-DG as a monotherapy, due to its poor drug-like characteristics, leadin
Externí odkaz:
https://doaj.org/article/0059a481e2a447b882323f913e1c01d8
Publikováno v:
Tetrahedron: Asymmetry. 13:2223-2228
The high-pressure intermolecular Diels–Alder reactions of sugar-derived dienes with N -phenylmaleimide are described and the crystal structure of a representative adduct is presented. The sugar matrix can be removed from the molecule, allowing the
Publikováno v:
Tetrahedron: Asymmetry. 12:1895-1905
The reaction of organometallic derivatives of monosaccharides with aldehydes catalyzed with BF3·OEt2 was studied. A significant difference in reactivity between the pyranosidic and furanosidic allyltins was noted. The former reacted readily with ald
Autor:
Stanisław Skóra, Sławomir Jarosz
Publikováno v:
Tetrahedron: Asymmetry. 12:1651-1656
Readily available unsaturated bicyclic ketones—obtained conveniently from sugar allyltins—are converted into highly oxygenated unsaturated decalins. The corresponding cis- and trans- diols resulting from oxidation of the double bond were obtained
Publikováno v:
Tetrahedron: Asymmetry. 11:1997-2006
The transformation of sugar allyltin derivatives into enantiomerically pure dienes (R*–CHCH–CHCH2) is presented. The internal double bond with the trans-configuration is formed regardless of the configuration of the starting sugar allyltin.
Autor:
Stanisław Skóra, Slawomir Jarosz
Publikováno v:
Tetrahedron: Asymmetry. 11:1433-1448
Preparation of enantiomerically pure, highly oxygenated decalins via tandem Wittig-type Diels–Alder reactions from the corresponding sugar-derived dieno-phosphoranes and/or -phosphonates and sugar aldehydes is described. Application of the phosphon
Autor:
Stanisław Skóra, Sławomir Jarosz
Publikováno v:
Tetrahedron: Asymmetry. 11:1425-1432
Tandem Wittig-type Diels–Alder reactions between sugar derived phosphonates and dienoaldehydes obtained from sugar allyltins lead, with high stereoselectivity, to complex oxygenated perhydroindene derivatives with the trans junction between the fiv
Publikováno v:
Journal of Carbohydrate Chemistry. 18:961-974
Reaction of sugar derived phosphonates [Sug-C(O)CH2P(O)(OMe)2] with sugar aldehydes (Sug'-CHO) provides the higher enones of the general formula Sug-C(O)CH=CH-Sug' with the trans configuration of the double bond. The phosphonate method is superior to
Publikováno v:
ChemInform. 31
Reaction of sugar derived phosphonates [Sug-C(O)CH2P(O)(OMe)2] with sugar aldehydes (Sug'-CHO) provides the higher enones of the general formula Sug-C(O)CH=CH-Sug' with the trans configuration of the double bond. The phosphonate method is superior to