P
Piotr Pawluć
Researcher at Adam Mickiewicz University in Poznań
Publications - 89
Citations - 1242
Piotr Pawluć is an academic researcher from Adam Mickiewicz University in Poznań. The author has contributed to research in topics: Catalysis & Silylation. The author has an hindex of 19, co-authored 83 publications receiving 949 citations. Previous affiliations of Piotr Pawluć include Wrocław University of Economics & university of lille.
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A Facile Synthesis of 1,1-Bis(silyl)ethenes.
TL;DR: In this article, a cyclic 1,1-bis(silyl)ethenes has been easily prepared via ruthenium complex-catalyzed silylative coupling cyclization of 1,2-bis (dimethylvinylsiloxy)ethane to give 2,2,4,4-tetramethyl-3-methylene-1,5-dioxa-2, 4-disilacycloheptane with excellent selectivity and good yield.
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1,4‐Bis[2,2‐bis(trimethylsilyl)ethenyl]benzene
TL;DR: The van der Waals inter-actions determine the crystal structure of the C22H42Si4 as mentioned in this paper, which is centrosymmetric in the sense that the molcules of the title compound are centroid symmetric.
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Highly Stereoselective Synthesis of N-Substituted π-Conjugated Phthalimides.
Piotr Pawluć,Adrian Franczyk,Jędrzej Walkowiak,Grzegorz Hreczycho,Maciej Kubicki,Bogdan Marciniec +5 more
TL;DR: In this article, a new regio-and stereoselective synthesis of (E)-N-(2-arylvinyl)phthalimides as well as phthalimide-containing (E,E)-buta-1,3-dienes and (E)but-1-en-3-ynes has been developed.
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(E)‐9‐(2‐Iodovinyl)‐9H‐carbazole: A New Coupling Reagent for the Synthesis of π‐Conjugated Carbazoles.
Piotr Pawluć,Adrian Franczyk,Jędrzej Walkowiak,Grzegorz Hreczycho,Maciej Kubicki,Bogdan Marciniec +5 more
TL;DR: Stereoselective silylative coupling of N-vinyl carbazole (I) followed by iododesilylation allows an easy access to the desired versatile building block (III) as mentioned in this paper.
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Mechanism of Silylation of Vinyl Arenes by Hydrodisiloxanes Driven by Stoichiometric Amounts of Sodium Triethylborohydride—A Combined DFT and Experimental Study
TL;DR: In this article , a simple transition-metal-free catalyst was used in the synthesis of silylation products, with flammable gaseous reagents replaced by a more convenient silane surrogate.