Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Wolfgang Bettray"'
Autor:
Tobias Horn, Wolfgang Bettray, Ulrike Noll, Felix Krauskopf, Meng-Ruo Huang, Carsten Bolm, Alan J. Slusarenko, Martin C. H. Gruhlke
Publikováno v:
Antioxidants, Vol 9, Iss 11, p 1086 (2020)
When cells of garlic (Allium sativum) are disrupted by wounding, they produce the defense substance allicin (diallylthiosulfinate). Allicin is an efficient thiol trap and readily passes through cell membranes into the cytosol, where it behaves as a r
Externí odkaz:
https://doaj.org/article/20e0d92163d64efa8644ea1c5125df50
Publikováno v:
Antioxidants, Vol 7, Iss 7, p 86 (2018)
Allicin (diallylthiosulfinate) is a potent thiol reagent and natural defense substance produced by garlic (Allium sativum) tissues when damaged. Allicin acts as a redox toxin and oxidizes the cellular glutathione (GSH) pool producing S-allylmercaptog
Externí odkaz:
https://doaj.org/article/8cc533c803a44d659ff30fd2c1c4f1a8
Autor:
Mihaela-D. Şerb, Wolfgang Wenzel, Melanie Homberger, Wolfgang Bettray, Frank Schiefer, Velimir Meded, Igor Beljakov, Ulrich Simon, Ulli Englert, Benjamin S. Gutrath
Publikováno v:
European Journal of Inorganic Chemistry. 2016:975-981
We present a detailed structural discussion of [Au8(PPh3)8](NO3)2, crystallized as a CH2Cl2 solvate. Its structure is compared with closely related triphenylphosphine-stabilized gold clusters. Characterization by optical extinction spectroscopy, lumi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dce18b17ee4c2d9bfd764205f18cc68e
https://doi.org/10.1002/ejic.201501334
https://doi.org/10.1002/ejic.201501334
Autor:
Wolfgang Bettray, Ulrike Noll, Felix Krauskopf, Tobias Horn, Martin C.H. Gruhlke, Carsten Bolm, Alan J. Slusarenko, Meng-Ruo Huang
Publikováno v:
Antioxidants
Volume 9
Issue 11
Antioxidants, Vol 9, Iss 1086, p 1086 (2020)
Antioxidants 9(11), 1086 (2020). doi:10.3390/antiox9111086 special issue: "Special Issue "Thiol-Based Redox Regulation of Cellular and Organismal Function" / Special Issue Editor: Prof. Dr. Bruce Morgan, Guest Editor"
Volume 9
Issue 11
Antioxidants, Vol 9, Iss 1086, p 1086 (2020)
Antioxidants 9(11), 1086 (2020). doi:10.3390/antiox9111086 special issue: "Special Issue "Thiol-Based Redox Regulation of Cellular and Organismal Function" / Special Issue Editor: Prof. Dr. Bruce Morgan, Guest Editor"
When cells of garlic (Allium sativum) are disrupted by wounding, they produce the defense substance allicin (diallylthiosulfinate). Allicin is an efficient thiol trap and readily passes through cell membranes into the cytosol, where it behaves as a r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::aedb7c1a59599bfb5019f0dcb1bf4547
https://doi.org/10.3390/antiox9111086
https://doi.org/10.3390/antiox9111086
Publikováno v:
Antioxidants 7(7), 86 (2018). doi:10.3390/antiox7070086 special issue: "Special Issue "Feature Papers in Antioxidants in 2018" / Guest Editor: Prof. Dr. Stanley Omaye, Department of Agriculture, Nutrition and Veterinary Sciences, University of Nevada, North Virginia"
Antioxidants, Vol 7, Iss 7, p 86 (2018)
Antioxidants
Volume 7
Issue 7
Antioxidants, Vol 7, Iss 7, p 86 (2018)
Antioxidants
Volume 7
Issue 7
Allicin (diallylthiosulfinate) is a potent thiol reagent and natural defense substance produced by garlic (Allium sativum) tissues when damaged. Allicin acts as a redox toxin and oxidizes the cellular glutathione (GSH) pool producing S-allylmercaptog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf2430aa81180c4cc55e5ea35dc6baf6
https://publications.rwth-aachen.de/record/728766
https://publications.rwth-aachen.de/record/728766
Autor:
Christoph Patzelt, Tanja Gulder, Alexander Pöthig, Wolfgang Bettray, Anna Ulmer, Maciej Stodulski, Stefanie V. Kohlhepp
Publikováno v:
Chemistry - A European Journal. 21:1444-1448
A tertiary hydroxy group α to a carboxyl moiety comprises a key structural motif in many bioactive substances. With the herein presented metal-free rearrangement of imides triggered by hypervalent λ(3)-iodane, an easy and selective way to gain acce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6ea7db9eb96abba8d023a363bb09a42
https://doi.org/10.1002/chem.201405888
https://doi.org/10.1002/chem.201405888
Publikováno v:
Synthesis. 2010:567-572
A microwave-assisted, organocatalytic domino Michael/Henry condensation/Michael/aldol condensation reaction has been developed. Employing acetaldehyde and nitroalkenes as substrates, this quadruple cascade allows an efficient asymmetric synthesis of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a5d401f41f604e5de862d8f24b05bc53
https://doi.org/10.1055/s-0029-1217146
https://doi.org/10.1055/s-0029-1217146
Autor:
Maciej Stodulski, Wolfgang Bettray, Christoph Patzelt, Stefanie V. Kohlhepp, Tanja Gulder, Anna Ulmer, Alexander Poethig
Publikováno v:
ChemInform. 46
The metal-free rearrangement of imides, catalyzed by in-situ formed trivalent iodine catalysts furnishes brominated α-hydroxycarboxylamides in high yields.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::86d2edbe12ea16742e084ec1a918953f
https://doi.org/10.1002/chin.201524087
https://doi.org/10.1002/chin.201524087
Publikováno v:
Tetrahedron. 58:2253-2329
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a73d6c0ae27ab5191bcb42c2138d296f
https://doi.org/10.1016/s0040-4020(02)00080-7
https://doi.org/10.1016/s0040-4020(02)00080-7
Publikováno v:
ChemInform. 44
It provides a simple, new, and highly enantioselective method to prepare a number of biologically important dihydropyridazines.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c7d2399a2dea0c97e633930cea98ea5d
https://doi.org/10.1002/chin.201351184
https://doi.org/10.1002/chin.201351184