Robert Bujok
Affiliations: | 2003-2005 | Warsaw University, Warszawa, mazowieckie, Poland |
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Stanek F, Pawlowski R, Morawska P, et al. (2020) Dehydrogenation and α-functionalization of secondary amines by visible-light-mediated catalysis. Organic & Biomolecular Chemistry. 18: 2103-2112 |
Wróbel Z, Tryniszewski M, Bujok R, et al. (2020) Reductive Condensation of a Nitro Group with Carboxylic Acids Promoted by Phosphorus(III) Compounds: A Short Route to 5H-Dibenzo[b,e][1,4]diazepin-11(10H)-ones Synthesis |
Bieniek M, Bujok R, Milewski M, et al. (2020) Making the family portrait complete: Synthesis of Electron Withdrawing Group activated Hoveyda-Grubbs catalysts bearing sulfone and ketone functionalities Journal of Organometallic Chemistry. 918: 121276 |
Tryniszewski M, Bujok R, Cmoch P, et al. (2019) Direct Reductive Cyclocondensation of the Nitro Group with the Amido Group: Key Role of the Iminophosphorane Intermediate in the Synthesis of 1,4-Dibenzodiazepine Derivatives. The Journal of Organic Chemistry. 84: 2277-2286 |
Bujok R, Mąkosza M. (2019) Synthesis of Diarylacetylenes Bearing Electron-Withdrawing Groups via the Smiles Rearrangement Synthesis. 51: 3109-3116 |
Bujok R, Wiszniewski M, Cmoch P, et al. (2018) A general and convenient method for the synthesis of 2,4-dinitrobenzyl ketones. Almost unlimited access to 2-substituted 6-nitroindoles from 2,4-dinitrotoluene and aldehydes New Journal of Chemistry. 42: 3260-3269 |
Bujok R, Cmoch P, Wróbel Z, et al. (2017) Transition-metal-free synthesis of 3-(1-pyrrolidinyl)quinolines and 3-(1-pyrrolidinyl)quinoline 1-oxides via a one-pot reaction of 3-(1-pyrrolidinyl)crotonates with nitrobenzenes. Organic & Biomolecular Chemistry |
Bujok R, Mąkosza M. (2016) Direct synthesis of nitroaryl acetylenes from acetylenes and nitroarenes via oxidative nucleophilic substitution of hydrogen. Chemical Communications (Cambridge, England) |
Wiȩcław M, Bobin M, Kwast A, et al. (2015) General synthesis of 2,1-benzisoxazoles (anthranils) from nitroarenes and benzylic C-H acids in aprotic media promoted by combination of strong bases and silylating agents. Molecular Diversity. 19: 807-16 |
Bujok R, Cmoch P, Wróbel Z. (2014) A novel annulation reaction of N-substituted-2-nitrosoanilines with esters of α-isocyano acids. A one-pot, two-step route to 2-benzimidazole- substituted esters of α-amino acids Tetrahedron Letters. 55: 3410-3413 |