Zobrazeno 1 - 10
of 108
pro vyhledávání: '"Jacek Skarżewski"'
Publikováno v:
Heteroatom Chemistry, Vol 2019 (2019)
New epoxides, derivatives of pyridine, 2,2′-bipyridine, and 1,10-phenanthroline, were synthesized from the respective α-methylazaarenes. The obtained racemic 2-oxiranyl-azaarenes along with styrene oxide and trans-stilbene oxide were submitted to
Externí odkaz:
https://doaj.org/article/5bea2b68838c41c0aadd6bb2a068358f
Publikováno v:
Molecules, Vol 26, Iss 12, p 3493 (2021)
Although many chiral ligands for asymmetric catalysis have been developed, there is still a need for new structures allowing the modular approach. Recently, easy synthesis of chiral pyridine-containing β-amino alcohols has been elaborated by opening
Externí odkaz:
https://doaj.org/article/ce6e0efb10144bf6a203b63a9ea686d9
Publikováno v:
ARKIVOC, Vol 2017, Iss 2, Pp 162-172 (2016)
Externí odkaz:
https://doaj.org/article/f0e44ef58abc44f4a6c7fd7af4f1b392
Publikováno v:
Molecules, Vol 25, Iss 21, p 4907 (2020)
New developments in the synthesis, resolution, and synthetic applications of chiral 1-phenylethylamine (α-PEA) reported in the last decade have been reviewed. In particular, improvements in the synthesis of α-PEA and its derivatives and chiral reso
Externí odkaz:
https://doaj.org/article/4535eb10208444168794695630c95b17
Publikováno v:
Molecules, Vol 25, Iss 3, p 727 (2020)
In this report, we describe the synthetic elaboration of the easily available enantiomerically pure β-amino alcohols. Attempted direct substitution of the hydroxyl group by azido-functionality in the Mitsunobu reaction with hydrazoic acid was ineffi
Externí odkaz:
https://doaj.org/article/7da0f628611847f6a7558f58b85c0e3d
Publikováno v:
ARKIVOC, Vol 2012, Iss 4, Pp 204-215 (2012)
Externí odkaz:
https://doaj.org/article/47893518da764d95a1110b336e5c4081
Autor:
Jim Küppers, Anna Christina Schulz-Fincke, Jerzy Palus, Mirosław Giurg, Jacek Skarżewski, Michael Gütschow
Publikováno v:
Pharmaceuticals, Vol 9, Iss 3, p 43 (2016)
The organo-seleniumdrug ebselen exhibits a wide range of pharmacological effects that are predominantly due to its interference with redox systems catalyzed by seleno enzymes, e.g., glutathione peroxidase and thioredoxin reductase. Moreover, ebselen
Externí odkaz:
https://doaj.org/article/d3eb05ff805745e293ce5e168731f9bf
Publikováno v:
Heteroatom Chemistry, Vol 2019 (2019)
New epoxides, derivatives of pyridine, 2,2′-bipyridine, and 1,10-phenanthroline, were synthesized from the respective α-methylazaarenes. The obtained racemic 2-oxiranyl-azaarenes along with styrene oxide and trans-stilbene oxide were submitted to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1678332180522b26d0f86de9f627ead3
https://doi.org/10.1155/2019/2381208
https://doi.org/10.1155/2019/2381208
Publikováno v:
Molecules, Vol 26, Iss 3493, p 3493 (2021)
Molecules
Volume 26
Issue 12
Molecules
Volume 26
Issue 12
Although many chiral ligands for asymmetric catalysis have been developed, there is still a need for new structures allowing the modular approach. Recently, easy synthesis of chiral pyridine-containing β-amino alcohols has been elaborated by opening
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4f536ce676fc998cc002037a5f273520
https://www.mdpi.com/1420-3049/26/12/3493
https://www.mdpi.com/1420-3049/26/12/3493
Publikováno v:
Molecules
Volume 25
Issue 3
Molecules, Vol 25, Iss 3, p 727 (2020)
Volume 25
Issue 3
Molecules, Vol 25, Iss 3, p 727 (2020)
In this report, we describe the synthetic elaboration of the easily available enantiomerically pure β-amino alcohols. Attempted direct substitution of the hydroxyl group by azido-functionality in the Mitsunobu reaction with hydrazoic acid was ineffi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f31b0b1f0608bebc054f20c832f92df