Nucleoside H-phosphonates. III. Chemical synthesis of oligodeoxyribonucleotides by the hydrogenphosphonate approachStereochemistry of internucleotide bond formation by the H-phosphonate method. 1. Synthesis and 31P NMR analysis of 16 diribonulceoside (3'-5')-H-phosphonates and the corresponding phosphorothioates.How to get the most out of two phosphorus chemistries. Studies on H-phosphonates.Minimal length of the lactose operator sequence for the specific recognition by the lactose repressor.The case of triethylammonium cation loss during purification of certain nucleotide analogues: a cautionary note.Recent advances in H-phosphonate chemistry. Part 1. H-phosphonate esters: synthesis and basic reactions.Searching for anti-glioma activity. Ribonucleoside analogues with modifications in nucleobase and sugar moieties.Aryl H-Phosphonates 18. Synthesis, properties, and biological activity of 2',3'-dideoxynucleoside (N-heteroaryl)phosphoramidates of increased lipophilicity.Synthesis and QSAR study of novel cytotoxic spiro[3H-indole-3,2'(1'H)-pyrrolo[3,4-c]pyrrole]-2,3',5'(1H,2'aH,4'H)-triones.Aryl nucleoside H-phosphonates. Part 16: synthesis and anti-HIV-1 activity of di-aryl nucleoside phosphotriesters.Aryl nucleoside H-phosphonates. Part 15: Synthesis, properties and, anti-HIV activity of aryl nucleoside 5'-alpha-hydroxyphosphonates.Aryl H-phosphonates 17: (N-aryl)phosphoramidates of pyrimidine nucleoside analogues and their synthesis, selected properties, and anti-HIV activity.Stereochemistry of internucleotide bond formation by the H-phosphonate method. 5. The role of Brønsted and H-bonding base catalysis in ribonucleoside H-phosphonate condensation-chemical and stereochemical consequences.O-Silylated C3-halohydrins as a novel class of protected building blocks for total, regio- and stereocontrolled synthesis of glycerolipid frameworks.Studies towards synthesis of dinucleoside arylphosphonates with metal complexing properties.9-Fluorenemethyl H-phosphonoselenoate--a versatile reagent for transferring an H-phosphonoselenoate group.Oxidative transformations of nucleoside fluorenemethyl H-phosphonoselenoate diesters.A cautionary note on the use of the 31P NMR spectroscopy in stereochemical correlation analysis.Regioselective and stereospecific acylation across oxirane- and silyloxy systems as a novel strategy to the synthesis of enantiomerically pure mono-, di- and triglycerides.Preparation of nucleoside H-phosphonoselenoate monoesters via the phosphinate approach.A proposal for a convenient notation for P-chiral nucleotide analogues. Part 2. Dinucleoside monophosphate analogues.A proposal for a new stereochemical notation for P-chiral nucleotide analogues and related compounds.A proposal for a convenient notation for P-chiral nucleotide analogues. Part 4. A relationship between the Dp/Lp notation and stereochemistry of reactions.New antiglioma zwitterionic pronucleotides with an FdUMP framework.Reaction of boranephosphonate diesters with amines in the presence of iodine: the case for the intermediacy of H-phosphonate derivatives.Regioselective and stereospecific cleavage of a terminal oxirane system: a novel synthetic approach to lipid mediator congeners--1,2(2,3)-diacyl-3(1)-halo-sn-glycerols.Nucleoside 3′,5′-Cyclic H-Phosphonates, New Useful Precursors for the Synthesis of Nucleoside 3′,5′-Cyclic Phosphates and Their AnaloguesComputational Study of the Mechanism and Selectivity of Palladium-Catalyzed Propargylic Substitution with Phosphorus NucleophilesNovel, Stereoselective and Stereospecific Synthesis of Allenylphosphonates and Related Compounds via Palladium-Catalyzed Propargylic SubstitutionSynthesis of Nucleotide Analogues with Pyridylphosphonate and Pyridylphosphono thio ate Internucleotide LinkagesStudies on the decomposition pathways of diastereoisomeric mixtures of aryl nucleoside α-hydroxyphosphonates under hydrolytic conditions. Synthesis of α-hydroxyphosphonate monoestersStereochemistry of internucleotide bond formation by the H-phosphonate method. 7. Stereoselective formation of ribonucleoside (RP)- and (SP)-3′-H-phosphonothioate monoestersChemical and Stereochemical Aspects of Oxidative Coupling of HPhosphonate and H-Phosphonothioate Diesters. Reactions with N,N-, N,Oand O,O-BinucleophilesEfficient synthesis of mono- and diarylphosphinic acids: a microwave-assisted palladium-catalyzed cross-coupling of aryl halides with phosphinateA New Reagent System for Efficient Silylation of Alcohols: Silyl Chloride-N-Methylimidazole-IodinePd(0)-Catalyzed Phosphorus−Carbon Bond Formation. Mechanistic and Synthetic Studies on the Role of the Palladium Sources and Anionic AdditivesSilylation-Mediated Transesterification ofO-Phenyl H-Phosphonothioates − A New Entry to Nucleoside H-Phosphonothioate MonoestersThe Case for the Intermediacy of Monomeric Metaphosphate Analogues during Oxidation ofH-Phosphonothioate,H-Phosphonodithioate, andH-Phosphonoselenoate Monoesters: Mechanistic and Synthetic StudiesH-Phosphonates: Versatile synthetic precursors to biologically active phosphorus compoundsStereospecific and regioselective opening of an oxirane system. A new efficient entry to 1- or 3-monoacyl- and 1- or 3-monoalkyl-sn-glycerols
P50
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P50
description
Polish chemist
@en
Polish chemist
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Polish chemist
@en-gb
Poola keemik
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Pools scheikundige
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ceimiceoir Polannach
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chimist polonez
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chimiste polonais
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kimist polak
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polnischer Chemiker
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name
Jacek Stawiński
@ast
Jacek Stawiński
@ca
Jacek Stawiński
@en
Jacek Stawiński
@es
Jacek Stawiński
@fr
Jacek Stawiński
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Jacek Stawiński
@nl
Jacek Stawiński
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Jacek Stawiński
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Jacek Stawiński
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type
label
Jacek Stawiński
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Jacek Stawiński
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Jacek Stawiński
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Jacek Stawiński
@es
Jacek Stawiński
@fr
Jacek Stawiński
@ga
Jacek Stawiński
@nl
Jacek Stawiński
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Jacek Stawiński
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Jacek Stawiński
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altLabel
Jacek Antoni Stawiński
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prefLabel
Jacek Stawiński
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Jacek Stawiński
@ca
Jacek Stawiński
@en
Jacek Stawiński
@es
Jacek Stawiński
@fr
Jacek Stawiński
@ga
Jacek Stawiński
@nl
Jacek Stawiński
@pl
Jacek Stawiński
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Jacek Stawiński
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P108
P214
P1053
C-6206-2009
P106
P108
P1207
P1559
Jacek Stawiński
@pl
P1695
P19
P21
P213
0000 0003 7369 734X
P214
P2381
P27
P31
P3124
P3829
P496
0000-0001-9350-3018
P569
1946-02-26T00:00:00Z