Jacek Stawiński - Concepedia

Author

Jacek Stawiński

Also Known As

J Stawinski, J Stawiński, J. STAWINSKI, J. Stawinski, J. Stawiński, J. Stawínski, Jacek Stawinski, Jacek Stawiński, M. Jezowska, Stawinski, J.

370

Publications

5.1K

Citations

H-Index

Concepts

All Affiliations

Stockholm University Institute of Bioorganic Chemistry, Polish Academy of Sciences Polish Academy of Sciences Plovdiv University

About

Jacek Stawiński is an author at Stockholm University specializing in chemistry, organic chemistry, and natural sciences.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Natural Sciences	30	75	2.8K
2	Biochemistry	26	64	2.2K
3	Engineering	25	56	2.2K
4	Medicine	8	8	301
5	Health Sciences	1	1	28

Jacek Stawiński

118

Publications

4.3K

Citations

H-Index

Page 1

	Year	Citations
Arylsulfonyltetrazoles, new coupling reagents and further improvements in the triester method for the synthesis of deoxyribooligonucleotides<sup>1</sup> Jacek Stawiński, Toyoharu Hozumi, Saran A. Narang, Nucleic Acids Research Combinatorial ChemistryBioorganic ChemistryEngineeringMolecular BiologyOrganic Chemistry	1977	234
Microwave-Assisted Palladium-Catalyzed Cross-Coupling of Aryl and Vinyl Halides with H-Phosphonate Diesters Asraa Ziadi, Jacek Stawiński Organic Letters	2008	182
Nucleoside H-phosphonates. III. Chemical synthesis of oligodeoxyribonucleotides by the hydrogenphosphonate approach Per J. Garegg, Ingvar Lindh, Tor Regberg, Tetrahedron Letters Nucleic Acid ChemistryBioorganic ChemistryBiochemistryNatural SciencesOligonucleotide	1986	171
Preparation of Arylphosphonates by Palladium(0)‐Catalyzed Cross‐Coupling in the Presence of Acetate Additives: Synthetic and Mechanistic Studies Martina Jezowska, Jacek Stawiński Advanced Synthesis & Catalysis Cross-coupling ReactionMechanistic StudiesEngineeringNatural SciencesAcetate Additives	2009	158
A general method for the synthesis of glycerophospholipids and their analogs via H-phosphonate intermediates Ingvar Lindh, Jacek Stawiński The Journal of Organic Chemistry Proteinlipid InteractionBioorganic ChemistryEngineeringChemical AnalysisAltmetric Attention Score	1989	130
Studies on aryl H-phosphonates. I. An efficient method for the preparation of deoxyribo- and ribonucleoside 3′-H-phosphonate monoesters by transesterification of diphenyl H-phosphonate Jadwiga Jankowska, Michał Sobkowski, Jacek Stawiński, Tetrahedron Letters Diphenyl H-phosphonateOrganic ChemistryChemistryAryl H-phosphonatesSynthetic Chemistry	1994	111
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 Adel S. Girgis, Jacek Stawiński, Nasser S. M. Ismail, European Journal of Medicinal Chemistry Natural SciencesMedicineDiversity-oriented SynthesisOrganic ChemistryChemistry	2011	108
Nucleoside H-phosphonates. IV. Automated solid phase synthesis of oligoribonucleotides by the hydrogenphosphonate approach Per J. Garegg, Inguar Lindh, Tor Regberg, Tetrahedron Letters Dna NanotechnologyBiochemistryNatural SciencesOligonucleotideMolecular Biology	1986	101
H-Phosphonates: Versatile synthetic precursors to biologically active phosphorus compounds Adam Kraszewski, Jacek Stawiński Pure and Applied Chemistry H- Phosphonate ChemistryBiosynthesisBioorganic ChemistryEngineeringBiochemistry	2007	87
Pd(0)-Catalyzed Phosphorus−Carbon Bond Formation. Mechanistic and Synthetic Studies on the Role of the Palladium Sources and Anionic Additives Jacek Stawiński Organometallics Materials ScienceInorganic ChemistryChemical EngineeringPossible PdEngineering	2007	85

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