Milosz Pawlicki
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Explore the profile of Milosz Pawlicki including associated specialties, affiliations and a list of published articles.
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48
Citations
353
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Recent Articles
1.
Dalberto K, Dzieszkowski K, Orzel L, Chmielewski P, Pawlicki M
Chempluschem
. 2024 Oct;
90(1):e202400636.
PMID: 39367790
An efficiency of delocalization in strongly conjugated systems remains an important factor crucial for modulation of the optical properties directly correlated with its range. An ortho-substituted phenylene derivative bearing electron...
2.
Banachowicz P, Das M, Kruczala K, Siczek M, Sojka Z, Kijewska M, et al.
Angew Chem Int Ed Engl
. 2024 Feb;
63(17):e202400780.
PMID: 38407458
A diradical/biradical character of organic derivatives is one of the key aspects of contemporary research focusing on the fundamental studies followed by potential applicability relying on the unique optical, electronic,...
3.
Hurej K, Oszczeda W, Opas E, Zelewski S, Pawlicki M, Bialek M, et al.
Angew Chem Int Ed Engl
. 2023 May;
62(28):e202303394.
PMID: 37178418
The insertion of palladium(II) into di-p-pyrirubyrin results in mutually convertible bimetallic complexes. Post-synthetic functionalization of one of them yielded bispalladium(II) dioxo-di-p-pyrirubyrin and, after demetallation, dioxo-di-p-pyrirubyrin, introducing for the first time...
4.
Peptide Stapling with Boronate Esters- A Reversible Folding of (Artificial) Peptide Chain to α-Helix
Kijewska M, Wolczanski G, Swiatowska M, Kedziora K, Pawlicki M, Stefanowicz P
Chemistry
. 2023 May;
29(40):e202301370.
PMID: 37148504
Stabilization of a peptide conformation via stapling strategy may be realized by the reversible or more often irreversible connection of side chains being in mutually appropriate geometry. An incorporation of...
5.
Li S, Sun Y, Li X, Smaga O, Koniarz S, Pawlicki M, et al.
Chem Commun (Camb)
. 2023 Mar;
59(25):3739-3742.
PMID: 36897336
A new group of aromatic porphyrinoids was obtained by an oxidative insertion of primary amines into the antiaromatic ring of 5,14-dimesityl-norcorrolatonickel(II) activated by iodosobenzene. The substituted 10-azacorroles thus formed were...
6.
Wypych K, Dimitrova M, Sundholm D, Pawlicki M
Org Lett
. 2022 Jul;
24(27):4876-4880.
PMID: 35796415
The macrocyclic structures with local conjugation readily undergo a redox-triggered change in the diatropic character, leading to a global current-density pathway of the doubly charged systems. The figure-eight geometry of...
7.
Farinone M, Kijewska M, Cybinska J, Siczek M, Pawlicki M
Chem Commun (Camb)
. 2022 Jun;
58(52):7269-7272.
PMID: 35674205
A logical construction of monomeric subunits armed with the carbonyl functionality allowing post-synthetic reactivity leads to the convergent formation of π-extended defected units activated with BBr. The kinetic or thermodynamic...
8.
Dutta A, Stawski W, Kijewska M, Pawlicki M
Org Lett
. 2021 Dec;
23(24):9436-9440.
PMID: 34870434
The 14π-electron system of anthracene has been merged with the unsaturated -1,2-difurylethene to form a macrocycle(s) with the retained local conjugation of all incorporated subunits that were substantially modulated with...
9.
Kijewska M, Siczek M, Pawlicki M
Org Lett
. 2021 Apr;
23(9):3652-3656.
PMID: 33856224
A macrocyclic motif composed of carbazole and pyridine subunits linked by a carbonyl bridge (C═O) forms a skeleton with a peripheral reactivity that leads to a pinacol-like coupling activated by...
10.
Ren D, Smaga O, Fu X, Li X, Pawlicki M, Koniarz S, et al.
Org Lett
. 2021 Jan;
23(3):1032-1037.
PMID: 33475380
A three-component reaction of antiaromatic -mesityl-3-nitronorcorrolatonickel(II) -NO with dialkyl acetylenedicarboxylate and PBu yields aromatic zwitterionic corrole nickel(II) complexes -R with one of the -substituents comprising a positively charged tributyl phosphonium...