about
The Elusive Paal-Knorr Intermediates in the Trofimov Synthesis of Pyrroles: Experimental and Theoretical Studies.Synthesis of novel aryl(heteroaryl)sulfonyl ureas of possible biological interest.Synthesis and in vitro anti-tumor activity of N-{1-[(3-thioxo-5,6-dihydroimidazo[2,1-c][1,2,4]thiadiazol-7-ylthio)thiocarbonyl]-2-imidazolidene}arylsulfonamides.Synthesis and Antifungal Activity of Some 4,6-Dimethylisoxazolo[3,4- b]pyridin-3(1H)-one Derivatives.Conjugate addition of nucleophiles to the vinyl function of 2-chloro-4-vinylpyrimidine derivatives.2-[(Arylmethoxy)imino]imidazolidines with potential biological activities.Carbon disulfide promoted reactions of 2-chloro-4,5-dihydro-imidazole with some N-nucleophiles.Synthesis, molecular structure, and applications of 2-hydroxylamino-4,5-dihydroimidazolium-O-sulfonate to the synthesis of novel heterocyclic ring systems.2-(4,5-dihydro-1H-imidazol-2-yl)indazole (indazim) derivatives as selective I(2) imidazoline receptor ligands.Synthesis and Structure-Activity Relationship Analysis of 5-HT₇ Receptor Antagonists: Piperazin-1-yl Substituted Unfused Heterobiaryls.1-[(Imidazolidin-2-yl)imino]-1H-indoles as new hypotensive agents: synthesis and in vitro and in vivo biological studies.Modifications of quinolones and fluoroquinolones: hybrid compounds and dual-action molecules.Copper(II)-assisted hydrolysis of cyclic ureas: Transformation of 1-(pyridin-2-yl)-2,3,7,8-tetrahydro-1 H -imidazo[2,1- b ][1,3,5]triazepin-5(6 H )-ones into N 1 -[1-(pyridin-2-yl)imidazolidin-2-ylidene]-ethane-1,2-diamine ligandsExperimental and theoretical studies on the tautomerism and reactivity of isoxazolo[3,4-b]quinolin-3(1H)-onesThe Tandem Mannich-Electrophilic Amination Reaction: a Versatile Platform for Fluorescent Probing and LabelingN-(Imidazolidin-2-ylidene)-1-arylmethanamine Oxides: Synthesis, Structure and Pharmacological EvaluationSynthesis and molecular structure of (Z)-1H-purin-6-ylideneaminooxysulfonic acid: a possible secondary metabolite of adenineSynthesis of aza-aromatic hydroxylamine-O-sulfonates and their application to tandem nucleophilic addition–electrophilic 5-endo-trig cyclizationSynthesis of Heterocycles by Intramolecular Nucleophilic Substitution at an Electron-Deficient sp2 Nitrogen AtomThe structure and theoretical study of 4-dimethylaminopyridinium N-(arylsulfonyl)carbamoylides2-Amino-4,5-dihydro-1H-imidazol-3-ium 7,8-dihydroimidazo[1,2-c][1,3,5]thiadiazine-2,4(6H)-dithione(1−) dimethylformamide disolvateFirst tandem nucleophilic addition–electrophilic amination reaction of Eschenmoser’s salts: synthesis of cyclic and spiro-fused hydrazonium saltsSynthesis, X-ray structure analysis and computational studies of novel bis(thiocarbamoyl) disulfides with non-covalent S⋯N and S⋯S interactionsSynthesis of 2,3-dihydroimidazo[1,2-a]pyrimidin-5(1H)-ones by the domino Michael addition retro-ene reaction of 2-alkoxyiminoimidazolidines and acetylene carboxylatesHydroxylamine-O-sulfonic AcidLipophilicity Determination of Quaternary (Fluoro)Quinolones by Chromatographic and Theoretical ApproachesLipophilicity Determination of Antifungal Isoxazolo[3,4-b]pyridin-3(1H)-ones and Their N1-Substituted Derivatives with Chromatographic and Computational MethodsSynthesis and biological evaluation of hybrid quinolone-based quaternary ammonium antibacterial agents
P50
Q38620581-516C73BB-4AC3-47D2-BDDB-9ECB844E7B56Q39723238-29542CF7-E8C6-429E-A98E-EA8874CCFE74Q40282516-DC1BEFDD-768E-41A9-9A15-BE55829010BBQ40672849-75E7E5D4-5275-4CBD-99D0-DA6D1EBC4672Q43119429-ABE439A7-4A18-409F-BC0C-C52220F2CD5CQ43202229-BA160274-4A60-4D95-AF8F-A73ABE766E16Q43738699-0894D3F8-ACC0-488B-A8B3-1114EB8D736BQ44468056-5FBFD05D-8A68-4BEA-815B-EF374DDBB984Q44612812-5D3B4B27-0A78-4DAA-8A8E-6ADA9EAAD13EQ48562904-12915AC7-F5EF-4D66-9D13-147E949B5E14Q51547753-1B50695B-C5C9-4849-B9FA-945D549DC012Q55407405-338C05C5-4D2A-47D3-94AC-75591A7E05ADQ58834214-2176DECC-B3A8-4C81-A064-415AFF59170BQ58834227-7F2526E4-FFCD-4658-B61D-DAB673ABE849Q58834255-42BB56F6-041A-44AE-A391-3D66B5B3B8FDQ58834260-CBCE54A7-0B33-4CED-AA04-C0F2D46009E5Q58834269-6B69DD5B-F592-4622-94DA-9450B9194040Q58834294-088B919F-4F78-44B4-A4C4-BB70E4C1E81AQ58834301-BE15433C-2B7C-4F60-86CC-1C6B55957FB4Q58834325-9BB76F44-A4CE-4EDE-B3D3-63C5DBEA93F2Q58834337-77E67BA9-262E-4BFF-8241-B4942AC7DF09Q58834340-3AC7267C-BB86-459B-BAFB-5FA6B878550EQ58834387-A7DA44E8-2293-4D07-AB7F-C95C8336FA27Q58834416-3CE8B6FA-3602-417D-9A93-A375ACE598D1Q60451447-D99FE88E-5C45-4AB6-8E2C-21A743360396Q90946774-64F64B1A-793D-413B-A82B-63CD9B93061AQ91513248-DE6995B0-6952-44FF-B966-BE6BF228B3E1Q91673557-E16E64BF-EC70-43B3-96A6-194B6123A0C7
P50
description
Polish chemist, researcher in medicinal chemistry
@en
Pools onderzoeker
@nl
cercetător polonez
@ro
chercheur polonais
@fr
investigador polaco
@es
investigador polaco
@gl
investigador polonès
@ca
polnischer Forscher
@de
polski chemik, zajmujący się chemią leków
@pl
ricercatore polacco
@it
name
Jarosław Sączewski
@ast
Jarosław Sączewski
@ca
Jarosław Sączewski
@de
Jarosław Sączewski
@en
Jarosław Sączewski
@es
Jarosław Sączewski
@fr
Jarosław Sączewski
@ga
Jarosław Sączewski
@gl
Jarosław Sączewski
@it
Jarosław Sączewski
@nl
type
label
Jarosław Sączewski
@ast
Jarosław Sączewski
@ca
Jarosław Sączewski
@de
Jarosław Sączewski
@en
Jarosław Sączewski
@es
Jarosław Sączewski
@fr
Jarosław Sączewski
@ga
Jarosław Sączewski
@gl
Jarosław Sączewski
@it
Jarosław Sączewski
@nl
altLabel
Jaroslaw Saczewski
@en
Jarosław Saczewski
@en
Saczewski J
@en
prefLabel
Jarosław Sączewski
@ast
Jarosław Sączewski
@ca
Jarosław Sączewski
@de
Jarosław Sączewski
@en
Jarosław Sączewski
@es
Jarosław Sączewski
@fr
Jarosław Sączewski
@ga
Jarosław Sączewski
@gl
Jarosław Sączewski
@it
Jarosław Sączewski
@nl
P1153
7801488667
P1412
P1559
Jarosław Sączewski
@pl
P21
P214
81152682555023312084
P27
P31
P3124
P496
0000-0003-2966-7645
P735
P7859
viaf-81152682555023312084