About: Wieslaw Prukała

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An Entity of Type : wikibase:Item, within Data Space : wikidata.demo.openlinksw.com associated with source document(s)

Polish chemist

Attributes	Values
rdf:type	Item
description	forskare (sv) ikertzailea (eu) 연구원 (ko) wetenschapper (nl) изилдөөчү (ky) 研究者 (zh) chimiste polonais (fr) Polish chemist (en) Poola keemik (et) chimist polonez (ro) kimist polak (sq) químic polonès (ca) químico polaco (es) químico polaco (gl) польський хімік (uk) כימאי פולני (he) كيميائي بولندي (ar) পোলীয় রসায়নবিদ (bn) polski chemik (chemia metaloorganiczna, chemia organiczna, kataliza kompleksami metali) (pl)
rdfs:label	Prukała W (nl) Wieslaw Prukała (en) Wiesław Prukała (pl)
skos:prefLabel	Prukała W (nl) Wieslaw Prukała (en) Wiesław Prukała (pl)
name	Prukała W (nl) Wieslaw Prukała (en) Wiesław Prukała (pl)
Polish scientist ID (deprecated)	wds:Q73166488-a0f8b3ac-4e47-977b-a255-ffb149450684
Polish scientist ID (deprecated)	14294
Scopus author ID	wds:Q73166488-61966037-A9F2-4DA5-9FAF-FB19560355EB
Scopus author ID	6507826164
given name	wds:Q73166488-4819FCEC-DFC9-48F1-BC1C-EF16A7811D75
given name	Wiesław
instance of	wds:Q73166488-0182711A-44F7-49D8-99AD-742823DED134
instance of	Homo sapiens
skos:altLabel	Prukała W (en) Wiesław Prukała (en)
occupation	wds:Q73166488-68E209FA-1E6E-4374-B0AC-289E2D6C2CCD wds:Q73166488-B4C905D9-E8B0-48A9-9C43-371EBDD38DF4
sex or gender	wds:Q73166488-ebfba92c-4960-4d41-177f-9e401114bc59
academic degree	wds:Q73166488-3522BD4A-6571-4687-AA59-45E62306A17E wds:Q73166488-92F0A060-CE32-411D-8711-36E8DC967736
educated at	wds:Q73166488-55AA306A-4E0E-4C5D-A4A2-971E2E13EF69
family name	wds:q73166488-8ffe28f7-4b3f-37a4-671f-192344fc4a0e
occupation	researcher chemist
sex or gender	male
academic degree	doctorate habilitation
educated at	Adam Mickiewicz University in Poznań
family name	Prukała
ORCID iD	wds:Q73166488-8D07CCD5-4BE9-4D17-B555-A41AAFEA8A8C
ORCID iD	https://orcid.org/0000-0001-9894-5771
ORCID iD	0000-0001-9894-5771
is about of	https://www.wikidata.org/wiki/Special:EntityData/Q73166488
is author of	Three 9-[(E)-2-(4-halogenophenyl)vinyl]-9H-carbazoles. Hydrogen-Bonded Complexes of Lumichrome Two 9-[(E)-nitrophenylvinyl]-9H-carbazoles Highly stereoselective synthesis, structure, and application of (E)-9-[2-(silyl)ethenyl]-9H-carbazoles COX-2 inhibitors: a novel strategy in the management of breast cancer Spectroscopy and photophysics of flavin-related compounds: 3-benzyl-lumiflavin New Applications and Analysis of (E)-Azastilbenes in Environmental Samples Two-dimensional EPR imaging with the rapid scan and rotated magnetic field gradient. Two-dimensional spectral-spatial EPR imaging with the rapid scan and modulated magnetic field gradient Spectroscopy and Photophysics of Lumiflavins and Lumichromes Analytics of Quinine and its Derivatives New photochemically stable riboflavin analogue—3-Methyl-riboflavin tetraacetate Electron ionization mass spectral study of selected N-amide and N-alkyl derivatives of cytisine. Antimicrobial activity of some N-alkyl and N-nitrobenzyl substituted halides of (E)-4'-hydroxy-3'-methoxystilbazoles-4 Synthesis, in vitro and in silico evaluation of novel trans-stilbene analogues as potential COX-2 inhibitors. Spectroscopy and photophysics of 9-methylalloxazine. Experimental and theoretical study Electron ionization and electrospray ionization mass spectrometric study of a series of isomeric N-chloro(or bromo)benzyl-substituted (E)-2'(3'- or 4')-hydroxy-4-stilbazole halides. Electron ionization mass spectrometric study of N-benzyl- and N-nitrobenzyl-substituted derivatives of cytisine. II. In search of excited-state proton transfer in the lumichrome dimer in the solid state: theoretical and experimental approach. Photophysical properties of izomeric N-chlorobenzyl substituted (E)-2' (3'-or 4')-hydroxy-4-stilbazolium chlorides in alcohols. Isomorphism in 1-(2-halidobenzyl)-4-[(E)-2-(3-hydroxyphenyl)ethenyl]pyridinium halide hemihydrates (halide = Cl, Br). Influence of water on photophysical properties of N-bromobenzyl- or nitrobenzyl derivatives of substituted 4-hydroxystilbazolium hemicyanines. Spectroscopy and photophysics of flavin-related compounds: 5-deaza-riboflavin Research on the Stability of Biologically Active (E)-azastilbene Derivatives in Polish Rivers Electron ionisation and electrospray ionisation mass spectrometric study of a series of isomeric methyl-, dimethyl- and trimethylalloxazines Influence of pH on photophysical properties of (E)-1-(4-chlorobenzyl)-4-(4-hydroxystyryl)pyridinium chloride. Two isomorphous azastilbene derivatives: 1-(2-chlorobenzyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]pyridinium chloride and 1-(2-bromobenzyl)-4-[(E)-2-(4-hydroxyphenyl)ethenyl]pyridinium bromide
is author of	wds:Q46867795-EA6F6CAC-5A59-4A95-9096-0719A98D88C3 wds:Q46739429-09A1C021-207A-4E03-B740-4983C4A3E515 wds:Q61352827-476D36AD-CEBB-40C5-85E1-5F106C12AADE wds:Q91016677-785FC753-A3AC-42B8-B778-6485B9BDB694 wds:Q38685004-1A66B0B0-3301-4242-A0F9-6F92F8D5C059 wds:Q46204880-A1D0348E-1FF5-4807-86DE-079E55DFE4B1 wds:Q50775402-728B7583-05F3-4A57-9450-2BDBA99EC556 wds:Q49390381-AD7F0E3E-2751-470B-B3B3-4F910FAA51BC wds:Q51004761-590F4C28-1B89-40AC-A04B-F2DD68133553 wds:Q61857263-F700A160-7335-4063-9805-F572272E0E06 wds:Q61857301-4260D8B2-0E03-42F1-9863-6749246A91BF wds:Q61857303-ED6CF005-EE1E-425E-8B75-AC99E8B60D07 wds:Q43137593-BB911800-76A1-4F9B-A7F0-CA6805014764 wds:Q46844607-0F7D404C-319A-4AA8-9B4F-31367216277F wds:Q50542398-F7F4ABBA-69B3-4960-8961-0CFBB8841D6B wds:Q46867724-5992245B-6527-48BF-9232-644A9598F409

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