Independent Work
18.
"Light-Driven Cobalt Hydride Catalyzed Hydroarylation
of Styrenes"
E. Bergamaschi+, V. J. Mayerhofer+, C. J. Teskey*
(+ authors contributed equally)
ACS Catal. 2022, 12, 14806–14811
(2nd most read paper in ACS Catalysis in December 2022, & selected as one of Hepatochem's top 22 photochemistry papers from 2022)
Highlighted in Synfacts here
17.
"Mild and Chemoselective Carboxylic Acid Reduction Promoted by Borane Catalysis"
D. Lunic, N. Sanosa, I. Funes-Ardoiz*, C. J. Teskey*
Angew. Chem. Int. Ed. 2022, 61, e202207647
(amongst the most accessed in September 2022
and highlighted in OPR&D)
"Light-Gated Cobalt(I) Hydride Catalysed Alkyne Hydroboration"
E. Bergamaschi & C. J. Teskey*
Tetrahedron Lett. 2022, 98, 153813
Invited submission in honor of Professor Dr Franziska Schoenebeck for the 2022 Tetrahedron Young Investigator Award in Organic Synthesis
16.
"Controlling Chemoselectivity of Catalytic Hydroboration
with Light"
E. Bergamaschi,+ D. Lunic,+ L. A. McLean, M. Hohenadel,
Y.-K. Chen, C. J. Teskey*
(+ authors contributed equally)
Angew. Chem. Int. Ed. 2022, 61, e202114482
Highlight in Synfacts here
15.
14.
"Dual Photoredox/Cobaloxime Catalysis for Cross-Dehydrogenative α-Heteroarylation of Amines"
E. Bergamaschi, C. Weike, V. J. Mayerhofer, I. Funes-Ardoiz*,
C. J. Teskey*
Org. Lett. 2021, 23, 5378–5382
(3rd most read article in Org. Lett. for August 2021)
13.
"Using Light to Modify Selectivity of Transition Metal Catalysed Transformations"
D. Lunic,+ E. Bergamaschi,+ C. J. Teskey*
(+ authors contributed equally)
12.
"Photocontrolled Cobalt Catalysis for Selective Hydroboration of α,β-Unsaturated Ketones"
F. Beltran,+ E. Bergamaschi,+ I. Funes-Ardoiz, C. J. Teskey*
(+ authors contributed equally)
Angew. Chem. Int. Ed. 2020, 59, 21176–21182
Highlight in Synfacts here
11.
"Visible-light controlled divergent catalysis using a bench-stable cobalt(I) hydride complex"
E. Bergamaschi,† F. Beltran,† C. J. Teskey* († authors contributed equally)
Postdoc & PhD Work
10.
"Alpha-functionalisation of ketones through metal-free electrophilic activation"
W. Zawodny, C. J. Teskey, M. Mishevska, M. Völkl,
B. Maryasin, L. González and N. Maulide*
Angew. Chem. Int. Ed. 2020, 59, 20935–20939
(amongst most accessed papers in Nov 2020)
"Unified Approach to the Chemoselective α-Functionalization of Amides with Heteroatom Nucleophiles"
C. R. Gonçalves,† M. Lemmerer,† C. J. Teskey,+ P. Adler,+ D. Kaiser,+ B. Maryasin, L. González, N. Maulide*
(†, + authors contributed equally)
J. Am. Chem. Soc. 2019, 141, 18437–18443
(2nd most read paper in Dec 2019)
9.
"α-Fluorination of carbonyls with nucleophilic fluorine"
P. Adler,†, C. J. Teskey,† D. Kaiser, M. Holy, H. H. Sitte, N. Maulide* (†authors contributed equally)
'Behind the paper' blog post here
8.
"Chemoselective α,β-Dehydrogenation of Saturated Amides"
C. J. Teskey,† P. Adler,† C. R. Gonçalves, N. Maulide*
(†authors contributed equally)
Angew. Chem Int. Ed. 2019, 58, 456–460
(a top 10% most downloaded paper in 2018-2019)
7.
“Regioselective synthesis of pyridines by redox alkylation of pyridine N-oxides with malonates”
M. Lemmerer, C. J. Teskey, D. Kaiser, N. Maulide*
6.
5.
“Ruthenium Catalyzed meta-Carboxylation”
H. L. Barlow, C. J. Teskey, M. F. Greaney*
“Chemoselective intermolecular cross-enolate-type coupling of amides”
D. Kaiser,† C. J. Teskey,† P. Adler, N. Maulide*
(†authors contributed equally)
J. Am. Chem. Soc. 2017, 139, 16040–16043
(3rd most read paper in Dec 2017)
4.
“Domino N- / C-Arylation via in situ generation of a directing group: An atom efficient approach to using diaryliodonium salts”
C. J. Teskey,† S. M. A. Sohel,† D. L. Bunting, S. G. Modha, M. F. Greaney* (†authors contributed equally)
Angew. Chem Int. Ed. 2017, 56, 5263–5266
(Hot Paper)
3.
“The Cross-Dehydrogenative-Coupling of Alkoxybenzenes with Toluenes: Copper(II) Halide Mediated Tandem Halo/Benzylation of Arenes”
T. E. Storr, C. J. Teskey, M. F. Greaney*
2.
“Ruthenium catalysed meta-selective C–H bond bromination”
C. J. Teskey, A. W. Y. Lui, M. F. Greaney*
Angew. Chem. Int. Ed. 2015, 54, 11677–11680
1.
