Head of the group
Prof. Bartłomiej Furman
Professors
Prof. Marek Chmielewski
Adjuncts
Dr. Piotr Szcześniak
Assistants
Dr. eng. Paweł Czerwiński
Chemists
Dr. Barbara Grzeszczyk
PhD students
M.Sc. eng. Justyna Najczuk
M.Sc. Magdalena Dolna
Head of the group
Prof. Bartłomiej Furman
Professors
Prof. Marek Chmielewski
Adjuncts
Dr. Piotr Szcześniak
Assistants
Dr. eng. Paweł Czerwiński
Chemists
Dr. Barbara Grzeszczyk
PhD students
M.Sc. eng. Justyna Najczuk
M.Sc. Magdalena Dolna
NCN Sonata 2019/35/D/ST4/00028 „Photochemical rearrangement of lactams: A ring-expansion approach towards structurally diverse heterocycles”
NCN OPUS (2019/35/B/ST4/02794) „Synthesis of structurally diverse medium- and large-sized rings by controlled decomposition of tetraoxanes and related compounds”
M. Chmielewski, R. Kutaszewicz, A. Ulikowski, M. Michalak, K. Wołosewicz, S. Stecko, B. Furman, „The Kinugasa Reaction”, Organic Reactions
P. Szcześniak, B. Furman, „Diversity-oriented synthesis of medium-sized cyclophanes via the photo-fries rearrangement of N-aryl lactams”, React. Chem. Eng.
M. Dolna, J. Narodowiec, O. Staszewska-Krajewska, P. Szcześniak, B. Furman, „Remotely controlled flow photo-Fries-type rearrangement of N-vinylazetidinones: An efficient route to structurally diverse 2,3-dihydro-4-pyridones”, React. Chem. Eng.
P. J. Czerwiński, B. Grzeszczyk, B. Furman, „Tertiary Amides as Fluoroalkyl Aldehyde Surrogates: Access to meso-Fluorinated Bis(heteroaryl)methanes”, Org. Lett.
P. J. Czerwiński, J. J. Najczuk, B. Furman, „From Flask to Mill: Reductive Functionalization of Fluoroacetamides as a Case Study for Transferring Solvent-Based Reactions to the Solid State”, ACS Sustainable Chem. Eng.
P. Szcześniak, B. Furman, „Photo-Fries-type rearrangement of cyclic enamides. An efficient route to structurally diverse five-membered enaminones”, Chem. Commun.
A. Domzalska-Pieczykolan, I. Funes-Ardoiz, B. Furman, C. Bolm, „Selective Approaches to α‐ and β‐Arylated Vinyl Ethers”, Angew. Chem. Int. Ed.
M. M. Więcław, B. Furman, „Direct synthesis of anomeric tetrazolyl iminosugars from sugar-derived lactams”, Beilstein J. Org. Chem.
P. Szcześniak, B. Grzeszczyk, B. Furman, „A Convenient Approach towards the Synthesis of ADMDP Type Iminosugars and Nojirimycin Derivatives from Sugar-Derived Lactams”, Molecules
P. Szcześniak, B. Furman, „Concise synthesis of bicyclic iminosugars via reductive functionalization of sugar-derived lactams and subsequent RCM reaction”, Org. Biomol. Chem.
P. Czerwiński, B. Furman, „Reductive Functionalization of Amides in Synthesis and for Modification of Bioactive Compounds”, Front. Chem.
O. Gawryś, M. Rak, I. Baranowska, S. Bobis-Wozowicz, K. Szaro, Z. Madeja, E. Kula-Świeżewska, M. Masnyk, M. Chmielewski, E. Karnas, E. Kompanowska-Jezierska, „Polyprenol-Based Lipofecting Agents for In Vivo Delivery of Therapeutic DNA to Treat Hypertensive Rats”, Biochem. Genet.
A. Domżalska-Pieczykolan, B. Furman, „Beyond the Tebbe Olefination: Direct Transformation of Esters into Ketones or Alkenes”, Synlett
B. Bujnicki, J. Błaszczyk, J. Drabowicz, M. Chmielewski, „Diastereoisomerically Pure, (S)-O-1,2-O-isopropyli dene-(5-O-α-d-glucofuranosyl) t-butanesulfinate: Synthesis, Crystal Structure, Absolute Configuration and Reactivity”, Molecules
M. Rak, A. Ochałek, K. Gawarecka, M. Masnyk, M. Chmielewski, T. Chojnacki, E. Kula-Świeżewska, Z. Madeja, „Boost of serum resistance and storage stability in cationic polyprenyl-based lipofection by helper lipids compositions”, Eur. J. Pharm. Biopharm.
B. Zambroń, „Internal Chelation within Functionalized Organoindium Reagents: Prospects for Regio- and Stereocontrol in the Allylation, Propargylation and Allenylation of Carbonyl Compounds”, Synthesis
P. Czerwiński, B. Furman, „A Long-Sought Reactivity of a Sodium Hydride”, Trends Chem.
P. Jankowski, R. Kutaszewicz, D. Ogończyk, P. Garstecki, „A microfluidic platform for screening and optimization of organic reactions in droplets”, J. Flow Chem.
O. Popik, B. Grzeszczyk, O. Staszewska-Krajewska, B. Furman, M. Chmielewski, „Synthesis of β-lactams via diastereoselective, intramolecular Kinugasa reactions”, Org. Biomol. Chem.
R. Kutaszewicz, B. Grzeszczyk, M. Górecki, O. Staszewska-Krajewska, B. Furman, M. Chmielewski, „Bypassing the stereoselectivity issue: transformations of Kinugasa adducts from chiral alkynes and non-chiral acyclic nitrones”, Org. Biomol. Chem.
P. Czerwiński, B. Furman, „Overcoming inaccessibility of fluorinated imines-synthesis of functionalized amines from readily available fluoroacetamides”, Chem. Commun.
P. Plata, B. Zambroń, S. Domin, „Diastereoselectivity Switch in the Pd(0)/InI-Mediated Reactions of β-Lactams with Aldehydes: An Entry into Nonracemic Semiprotected (3 E)-2,6-Enediols”, J. Org. Chem.
B. Zambroń, S. Domin, J. Kędzierski, „Remote 1,5-Stereoselectivity Control by an N-Ligand Switch in the Pd(0)/InI-Promoted Reactions of 4-Ethynyl-β-lactams with Aldehydes”, Org. Lett.
K. Kabala, B. Grzeszczyk, B. Furman, M. Chmielewski, J. Solecka, A. Guśpiel, „Synthesis of Monobactams via the Diastereoselective Kinugasa Reaction”, Synthesis
B. Szechner, A. Jaromin, S. Parapini, N. Basilico, B. Grzeszczyk, B. Furman, M. Chmielewski, „Glycosyl hydroperoxides: A new class of potential antimalarial agents”, Bioorg. Med. Chem.
P. Plata, U. Klimczak, B. Zambroń, ”Acyclic Remote 1,5- and 1,4,5-Stereocontrol in the Catalytic Stereoselective Reactions of β-Lactams with Aldehydes: The Effect of the N-Methylimidazole Ligand”, J. Org. Chem.
P. Szcześniak, O. Staszewska-Krajewska, B. Furman, J. Młynarski, „Solid supported Hayashi–Jørgensen catalyst as an efficient and recyclable organocatalyst for asymmetric Michael addition reactions”, Tetrahedron: Asymmetry
A. Domżalska, E. Maziarz, B. Furman, „A new synthesis of highly functionalized cyclohexenes via a vinylogous Ferrier-Petasis cyclization reaction”, Tetrahedron
M. Pieczykolan, B. Furman, M. Chmielewski, „Formal synthesis of Thienamycin”, J. Antibiot.
P. Szcześniak, O. Staszewska-Krajewska, B. Furman, J. Młynarski, „Asymmetric Synthesis of Cyclic Nitrones via Organocatalytic Michael Addition of Aldehydes to Nitroolefins and Subsequent Reductive Cyclization”, Chemistry Select
G. Lipner, A. Ulikowski, A. Domżalska, B. Furman, „Flexible synthesis of fused piperidinones and application in the synthesis of (+/-)-myrtine”, Tetrahedron
M. Pieczykolan, O. Staszewska-Krajewska, B. Furman, M. Chmielewski, „1,3-Dipolar cycloaddition of a cyclic nitrone derived from 2-deoxy-D-ribose to alpha,beta-unsaturated lactones: An entry to carbapenem antibiotics”, Carbohydr. Res.
P. Szcześniak, A. Ulikowski, O. Staszewska-Krajewska, G. Lipner, B. Furman, „Stereoselective synthesis of benzoquinolizidines and related homologues via intramolecular addition to dihydropyridones”, Tetrahedron
K. Wolosewicz, M. Michalak, J. Adamek, B. Furman, “Studies on the Enantioselective Kinugasa Reaction: Efficient Synthesis of beta-Lactams Catalyzed by N-PINAP/CuX Complexes”, Eur. J. Org. Chem.
M. Soluch, B. Grzeszczyk, O. Staszewska-Krajewska, M. Chmielewski, B. Furman, „Synthesis of Thienamycin methyl ester from 2-deoxy-D-ribose via Kinugasa reaction”, J. Antibiot.
A. Ulikowski, B. Furman, „Schwartz’s Reagent-Mediated Regiospecific Synthesis of 2,3-Disubstituted Indoles from Isatins”, Org. Lett.
L. Mucha, K. Parda, O. Staszewska-Krajewska, S. Stecko, A. Ulikowski, J. Frelek, A. Suszczyńska, M. Chmielewski, B. Furman, „Diastereoselective synthesis of beta-lactams via Kinugasa reaction of acyclic chiral nitrones”, Tetrahedron: Asymmetry