Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Oskar Popik"'
Autor:
Karol Molga, Sara Szymkuć, Patrycja Gołębiowska, Oskar Popik, Piotr Dittwald, Martyna Moskal, Rafal Roszak, Jacek Mlynarski, Bartosz A. Grzybowski
Publikováno v:
Nature Synthesis. 1:49-58
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::511cb57dd0e0e35ec73246943e0d51d9
https://doi.org/10.1038/s44160-021-00010-3
https://doi.org/10.1038/s44160-021-00010-3
Autor:
Karl A. Scheidt, Patrycja Gołębiowska, Wiktor Beker, Olga Staszewska-Krajewska, Oskar Popik, Bartosz A. Grzybowski, Karol Molga, Ewa P. Gajewska, Milan Mrksich, Tomasz Badowski, Sara Szymkuć, Piotr Dittwald, Alison A. Bayly, Barbara Mikulak-Klucznik, Tomasz Klucznik, Jacek Mlynarski
Publikováno v:
Nature. 588:83-88
Training algorithms to computationally plan multistep organic syntheses has been a challenge for more than 50 years1-7. However, the field has progressed greatly since the development of early programs such as LHASA1,7, for which reaction choices at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43b49ec33d29fc332cc80fc341d21d40
https://doi.org/10.1038/s41586-020-2855-y
https://doi.org/10.1038/s41586-020-2855-y
Autor:
Sara Szymkuć, Bartosz A. Grzybowski, Jacek Mlynarski, Michał Startek, Ewa P. Gajewska, Oskar Popik, Piotr Dittwald
Publikováno v:
Chem. 6:280-293
Summary Whereas most organic molecules can be synthesized from progressively simpler substrates, syntheses of complex organic targets often involve counterintuitive sequence of steps that first complexify the structure but, by doing so, open up possi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::888c6477332f561930f50b63d07d0fbb
https://doi.org/10.1016/j.chempr.2019.11.016
https://doi.org/10.1016/j.chempr.2019.11.016
Autor:
Oskar Popik, Adam S. Hogendorf, Mikołaj Matłoka, Rafal Moszczynski, Agnieszka Nikiforuk, Agnieszka Potasiewicz, Piotr Popik, Joanna Golebiowska, Jeffrey M. Witkin, Agata Kuziak, Shaun Yon-Seng Khoo
Although (S)-ketamine was approved for use in treatment-resistant depression in 2019, new preclinical findings suggest that (R)-ketamine might produce better efficacy and tolerability relative to (S)-ketamine. Here we evaluated the effects of (R)-, (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2a0f4c1a98b634c8feec99d9671ff685
https://doi.org/10.1016/j.pbb.2020.173011
https://doi.org/10.1016/j.pbb.2020.173011
Autor:
Bartłomiej Furman, Olga Staszewska-Krajewska, Marek Chmielewski, Oskar Popik, Barbara Grzeszczyk
Publikováno v:
Organicbiomolecular chemistry. 18(15)
Intramolecular Kinugasa reactions on in situ generated carbohydrate-derived alkynylnitrones are described. The effects of the length of chains, their mutual configuration, influence of experimental conditions on product distribution and feasibility o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5bd92e41b1f043d3a59df2484da485b
https://pubmed.ncbi.nlm.nih.gov/32211731
https://pubmed.ncbi.nlm.nih.gov/32211731
Publikováno v:
ChemistryOpen
Herein we report a short and efficient protocol for the synthesis of naturally occurring higher‐carbon sugars—sedoheptulose (d‐altro‐hept‐2‐ulose) and d‐glycero‐l‐galacto‐oct‐2‐ulose—from readily available sugar aldehydes an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c3e98eb4696bbe5ddbaf2f67f882be3
https://doi.org/10.1002/open.201500099
https://doi.org/10.1002/open.201500099
The synthesis of a legionaminic acid donor from N-acetyl neuraminic acid in fifteen steps and 17% overall yield is described. Activation of the adamantanyl thioglycoside in the donor with N-iodosuccinimide and trifluoromethanesulfonic acid in dichlor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::acb26c7cb5ea4ffddefef5e510e87572
https://europepmc.org/articles/PMC5545936/
https://europepmc.org/articles/PMC5545936/
Autor:
Marcin Górecki, Magdalena Jawiczuk, Jadwiga Frelek, Monika Pasternak-Suder, Oskar Popik, Jacek Mlynarski, Katarzyna Leśniak
Publikováno v:
The Journal of organic chemistry. 79(12)
This article presents comprehensive studies on the application of primary, secondary, and tertiary amines as e ffi cient organocatalysts for the de novo synthesis of ketoses and deoxyketoses. Mimicking the actions of aldolase enzymes, the synthesis o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df708499b182afc56df1f4b2ca8f038a
https://pubmed.ncbi.nlm.nih.gov/24837738
https://pubmed.ncbi.nlm.nih.gov/24837738
Publikováno v:
ChemInform. 45
It is found that the serinamides (SBS) and (RBS) efficiently promote highly enantioselective syn-selective reaction of dihydroxyacetone with diverse aldehydes including optically pure ones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5bd412bc5a1bf26f271abd540c16b256
https://doi.org/10.1002/chin.201418212
https://doi.org/10.1002/chin.201418212