Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Marcin Budny"'
Publikováno v:
Organic Letters. 23:5123-5127
The synthesis of 1,2,4-triazolium tetrafluoroborates under electrochemical conditions is reported. The reaction is performed with stoichiometric amounts of HBF4, which converts starting materials to their corresponding cationic forms due to protonati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ff228843284ab70a5c48efb0dac0ffe2
https://doi.org/10.1021/acs.orglett.1c01651
https://doi.org/10.1021/acs.orglett.1c01651
Autor:
Marcin Budny, Małgorzata Wysocka, Joanna Andrusiak, Andrzej Wolan, Jacek Ścianowski, Kinga Mylkie
Publikováno v:
RSC Advances. 11:28934-28939
A six-step synthesis of xanthohumol (1a) and its d3-derivative (1b) from easily accessible naringenin is reported. The prenyl side chain was introduced by Mitsunobu reaction followed by the europium-catalyzed Claisen rearrangement and base-mediated o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::535aaca29c5c7d4943df3037f6d69cca
https://doi.org/10.1039/d1ra05443k
https://doi.org/10.1039/d1ra05443k
Autor:
Joanna, Andrusiak, Kinga, Mylkie, Małgorzata, Wysocka, Jacek, Ścianowski, Andrzej, Wolan, Marcin, Budny
Publikováno v:
RSC advances. 11(46)
A six-step synthesis of xanthohumol (1a) and its d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c9e852b65a95137e8e2146741dcb889f
https://pubmed.ncbi.nlm.nih.gov/35478583
https://pubmed.ncbi.nlm.nih.gov/35478583
Autor:
J.I. Loch, Anna Ciarkowska, Zuzanna Sokolowska, Marcin Budny, Magdalena Wujak, Magdalena Barwiolek, Anna Kozakiewicz, Andrzej Wojtczak
Publikováno v:
International Journal of Molecular Sciences, Vol 22, Iss 5541, p 5541 (2021)
International Journal of Molecular Sciences
Volume 22
Issue 11
International Journal of Molecular Sciences
Volume 22
Issue 11
Statins are the most effective cholesterol-lowering drugs. They also exert many pleiotropic effects, including anti-cancer and cardio- and neuro-protective. Numerous nano-sized drug delivery systems were developed to enhance the therapeutic potential
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0831a4b0815c2a4a5894053980013c36
https://www.mdpi.com/1422-0067/22/11/5541
https://www.mdpi.com/1422-0067/22/11/5541
Publikováno v:
Tetrahedron Letters. 58:4285-4288
The stereoselective synthesis of compounds 5 and 6, potential hydroxylated metabolites of the agricultural fungicide cis-metconazole, is reported. In a key step of the initially surveyed synthetic route, hydrodechlorination of 12 was competitive with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2d02c5099cbc3ad6b2a76849b536678
https://doi.org/10.1016/j.tetlet.2017.09.087
https://doi.org/10.1016/j.tetlet.2017.09.087
Publikováno v:
Tetrahedron Letters. 56:6093-6096
A six step conversion of the common carbocyclic nucleoside precursor 8 into the all-cis key intermediate for the synthesis of ticagrelor analogs is reported. The method involves two oxidation/stereoselective reduction sequences for both the C O and C
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::728d7ccb860e928a1621603fca3c9a92
https://doi.org/10.1016/j.tetlet.2015.09.074
https://doi.org/10.1016/j.tetlet.2015.09.074
Publikováno v:
European Journal of Organic Chemistry. 2014:6361-6365
Rhodium-catalyzed cyclization of N-(2,3,4,5,6-pentafluoro-benzyloxy) diazo amides leading to the corresponding γ-lactams is described. The cyclization is based on the intramolecular catalytic insertion into the C–H bond. Fourteen lactams were obta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e25a5d86f0518670df8ecb97f569319
https://doi.org/10.1002/ejoc.201402571
https://doi.org/10.1002/ejoc.201402571
Publikováno v:
Tetrahedron Letters. 52:1195-1198
A facile zinc-mediated Barbier-type allylation of aromatic aldoxime esters, producing the corresponding protected homoallylic hydroxylamines, which are readily converted into homoallylic hydroxamic acids, is described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09bce8479c4f1657459dee808909ee52
https://doi.org/10.1016/j.tetlet.2011.01.032
https://doi.org/10.1016/j.tetlet.2011.01.032
Publikováno v:
ChemInform. 46
A series of diazo amides bearing the -Fbo protecting group is successfully cyclized to γ-lactam structures with different yields and stereoselectivities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::082b69fbf7fc2b30de7604798c28edbd
https://doi.org/10.1002/chin.201513169
https://doi.org/10.1002/chin.201513169
Publikováno v:
ChemInform. 42
The title reaction proceeds under Barbier conditions to afford the corresponding homoallylic hydroxylamine esters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e28f6f712ffd0bd1cc69420cdb7eb963
https://doi.org/10.1002/chin.201119080
https://doi.org/10.1002/chin.201119080