Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Grzegorz Pikus"'
Publikováno v:
ARKIVOC, Vol 2017, Iss 2, Pp 534-545 (2017)
Externí odkaz:
https://doaj.org/article/69052496ba954983b609de13795e45f4
Publikováno v:
Molecules, Vol 24, Iss 14, p 2635 (2019)
Three (R)-BINOL-based macrocyclic receptors obtained via double-amidation reaction were used for chiral recognition of four anions derived from α-hydroxy and α-amino acids. The structural factors of hosts and guests that affect chiral recognition p
Externí odkaz:
https://doaj.org/article/60723d5ca7bf4fb4a1c62a018861f1b6
Autor:
Kamil Kopeć, Agata Ryżko, Roman Major, Hanna Plutecka, Justyna Wiȩcek, Grzegorz Pikus, Jakub W. Trzciński, Adrianna Kalinowska, Tomasz Ciach
Publikováno v:
ACS Omega. 7:39234-39249
Surface properties are crucial for medical device and implant research and applications. We present novel polycatecholamine coatings obtained by oxidative polymerization of l-tyrosine, l-phenylalanine, and 2-phenylethylamine based on mussel glue-insp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a8dba54b07d4fd51dd3d6f85965aee9
https://doi.org/10.1021/acsomega.2c05289
https://doi.org/10.1021/acsomega.2c05289
Publikováno v:
ACS Combinatorial Science
We investigated the yield and distribution of macrocyclic products formed in combinatorial libraries (CLs) obtained via double-amidation reactions of methyl diesters with α,ω-diamines. The application of the static combinatorial chemistry (SCC) app
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0433f71e249de44a506eaa80b6785bf1
http://europepmc.org/articles/PMC7588042
http://europepmc.org/articles/PMC7588042
Publikováno v:
The Journal of Organic Chemistry. 84:6502-6507
Five BINOL-based hosts with a variable macroring size were synthesized in a two-step postfunctionalization protocol by double N-benzylation followed by BMS-mediated reduction of tertiary amide groups (53–93%). UV–vis titration in MeCN reveals tha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93493a9418eb33e9badcd9aa8365c990
https://doi.org/10.1021/acs.joc.9b00630
https://doi.org/10.1021/acs.joc.9b00630
Autor:
Kamil Brygoła, Konstancja Kopyra, Urszula Karczmarczyk, Tomasz Ciach, Jolanta Duszak, Michał Szkop, Magdalena Janczewska, Anna Świątkowska, Michał Żuk, Grzegorz Pikus, Jarosław Walczak
Publikováno v:
Applied radiation and isotopes : including data, instrumentation and methods for use in agriculture, industry and medicine. 167
Background Currently, radiotherapy is one of the most popular choices in clinical practice for the treatment of cancers. While it offers a fantastic means to selectively kill cancer cells, it can come with a host of side effects. To minimize such sid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7acd2dddabc13ee0a6f55a6b831e361b
https://pubmed.ncbi.nlm.nih.gov/33086151
https://pubmed.ncbi.nlm.nih.gov/33086151
Publikováno v:
ARKIVOC, Vol 2017, Iss 2, Pp 534-545 (2017)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c327cd30de6b995928e43827e327fd0e
https://doi.org/10.24820/ark.5550190.p009.824
https://doi.org/10.24820/ark.5550190.p009.824
Autor:
Grzegorz Pikus, Janusz Jurczak
Publikováno v:
Tetrahedron. 72:1928-1932
Double-amidation reaction of (R)- or (S)-2,2′-([1,1′-binaphthalene]-2,2′-diylbis(oxy))diacetic dimethyl ester with five differing in length α,ω-diaminoethers were used for the synthesis of chiral macrocyclic compounds of different size of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43e14b51614a77f865432b6356f2d004
https://doi.org/10.1016/j.tet.2016.02.051
https://doi.org/10.1016/j.tet.2016.02.051
Publikováno v:
Tetrahedron. 76:131438
In this work we presented two-, three-, and four-substrate static combinatorial libraries (SCLs) obtained via macrocyclization of BINOL-based dimethyl ester and five α,ω-diaminoethers of varying lengths. We investigated the distribution of macrocyc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a964e968921342c7ee2ae1d57b97dd18
https://doi.org/10.1016/j.tet.2020.131438
https://doi.org/10.1016/j.tet.2020.131438