Wojciech Chaładaj

Kierownik zespołu
dr hab. Wojciech Chaładaj, prof. IChO PAN

Asystenci
Dr inż. Maciej Dajek

Doktoranci
M.Sc. Prachi Shah
M.Sc. Shrenik Sheth

NCN OPUS 2019/35/B/ST4/00599
„Kontrola regio- i stereoselektywności hydro- i karbofluorometylowania poprzez sekwencję hydro- lub karbometalowania i funkcjonalizację C-M”

K. Grudzień, Z. Szeptuch, H. Kubiszewski, W. Chaładaj, K. Rybicka-Jasińska, „NHC-Cu Three-Coordinate Complex as a Promising Photocatalyst for Energy and Electron Transfer Reactions”, J. Org. Chem.

B. Bisek, K. Kochaniak, W. Chaładaj, „Lithium Enables Pd-Catalyzed 5-endo-dig Cyclization/Coupling of α-Homopropargyl-β-ketoesters with Aryl Bromides and Triflates”, Org. Lett.

M. Bao, K. Łuczak, W. Chaładaj, M. Baird, D. Gryko, M. P. Doyle, „Photo-cycloaddition reactions of vinyldiazo compounds”, Nat. Commun.

M. Wosińska-Hrydczuk, M. Yaghoobi-Anzabi, J. Przedziecki, O. Danylyuk, W. Chaładaj, D. Gryko, „Unique Reactivity of Triazolyl Diazoacetates under Photochemical Conditions”, ACS Org. Inorg. Au

B. Bisek, W. Chaładaj, „Access to 2-Alkenyl-furans via a Cascade of Pd-Catalyzed Cyclization/Coupling Followed by Oxidative Aromatization with DDQ”, J. Org. Chem.

G. Sanil, M. Krzeszewski, W. Chaładaj, W. Danikiewicz, I. Knysh, Ł. Dobrzycki, O. Staszewska-Krajewska, M. Cyrański, D. Jacquemin, D. T. Gryko, „Unprecedented 1,2-Aryl Shift Accompanying Double Alkyne Benzannulation”, Angew. Chem. Int. Ed.

A. Błocka,   J. Ostapko, W. Chaładaj, „Tandem Pd-catalyzed annulation/coupling of acetylenic enamines with aryl triflates”, Chem. Commun.

F. Lucio-Martínez, W. Chaładaj, „Fluoroalkyl Iodides in Fluoroalkylative Difunctionalization of C−C Multiple Bonds”, Adv. Synth. Catal.

K. Orłowska, J. V. Santiago, P. Krajewski, K. Kisiel, I. Deperasińska, K. Zawada, W. Chaładaj, D. Gryko, „UV Light Is No Longer Required for the Photoactivation of 1,3,4-Oxadiazolines”, ACS Catal.

B. Bisek, W. Chaładaj, „Controllable Access to Furans and Dihydrofurans through Cyclization/Coupling of Internal Acetylenic β-Ketoesters with Aryl Bromides”, Adv. Synth. Catal.

A. Błocka, W. Chaładaj, „Tandem Pd-Catalyzed Cyclization/Coupling of Non-Terminal Acetylenic Activated Methylenes with (Hetero)Aryl Bromides”, Molecules

A. Potrząsaj, M. Ociepa, W. Chaładaj, D. Gryko, „Bioinspired Cobalt-Catalysis Enables Generation of Nucleophilic Radicals from Oxetanes”, Org. Lett.

B. Gatlik, W. Chaładaj, „Pd-Catalyzed Perfluoroalkylative Aryloxycarbonylation of Alkynes with Formates as CO Surrogates”, ACS Catal.

A. Potrząsaj, M. Musiejuk, W. Chaładaj, M. Giedyk, D. Gryko, „Cobalt Catalyst Determines Regioselectivity in Ring Opening of Epoxides with Aryl Halides”, J. Am. Chem. Soc.

N. Upadhyay, W. Chaładaj, „Palladium‐Catalyzed Carboperfluoroalkylation of Alkynes with Fluoroalkyl Iodides and Arylstannanes”, Adv. Synth.Catal.

A. Błocka, P. Woźnicki, M. Stankevič, W. Chaładaj, „Pd-catalyzed intramolecular addition of active methylene compounds to alkynes with subsequent cross-coupling with (hetero)aryl halides”, RSC Adv.

S.Domański, B.Gatlik, W. Chaładaj, „Pd-Catalyzed Boroperfluoroalkylation of Alkynes Opens a Route to One-Pot Reductive Carboperfluoroalkylation of Alkynes with Perfluoroalkyl and Aryl Iodides”, Org. Lett.

A. Kołodziejczyk, S. Domański, W. Chaładaj, „Tandem Palladium-Catalyzed 6-exo-dig Oxocyclization-Coupling of δ-Acetylenic-β-ketoesters with Aryl Bromides and Chlorides: Efficient Route to Substituted Dihydropyrans”, J. Org. Chem.

A. Kołodziejczyk, W. Chaładaj, „Efficient and Functional‐Group‐Tolerant Synthesis of Substituted Furans through the Pd‐Catalyzed 5‐exo‐dig Cyclization/Coupling of γ‐Acetylenic β‐Keto Esters with (Hetero)Aryl Bromides”, Eur. J. Org. Chem.

M. Kocój, E. Jarosińska, W. Chaładaj, „High-pressure Au-catalyzed cycloisomerization of internal 1,6- and 1,7-enynes”, Synlett

W. Chaładaj, A. Kołodziejczyk, S. Domański, „Gold(I)-Catalyzed Conia-ene Cyclization of Internal ϵ-Acetylenic β-Ketoesters under High Pressure.”, ChemCatChem

S. Domański, O. Staszewska-Krajewska, W. Chaładaj, Pd-Catalyzed Carbonylative Carboperfluoroalkylation of Alkynes. „Through-Space 13C–19F Coupling as a Probe for Configuration Assignment of Fluoroalkyl-Substituted Olefins.”, J. Org. Chem.

M. Białkowska, W. Chaładaj, I. Deperasińska, A. Drzewiecka-Antonik, A. E. Koziol, A. Makarewicz, B. Kozankiewicz, „Single molecules of terrylene in di-substituted naphthalenes crystallizing in the herringbone pattern.”, RSC Adv.

S. Domański, W. Chaładaj, „A Broadly Applicable Method for Pd-Catalyzed Carboperfluoro-alkylation of Terminal and Internal Alkynes: A Convenient Route to Tri- and Tetrasubstituted Olefins”, ACS Catal.
Praca wyróżniona w: Synfacts 2016, 12, 842.

W. Chaładaj, S. Domański, „Mild and Functional Group Tolerant Method for Tandem Palladium-Catalyzed Carbocyclization–Coupling of ε-Acetylenic β-Ketoesters with Aryl Bromides and Chlorides”, Adv. Synth. Catal.