Top Ten Papers

Personal Reference, Most Recent First

1.   Photoredox catalysis with aryl sulfonium salts enables site-selective late-stage fluorination

J. Li, J. Chen, R. Sang, W.S. Ham, M.B. Plutschack, F. Berger, S. Chabbra, A. Schnegg, C. Genicot, T. Ritter “Photoredox catalysis with aryl sulfonium salts enables site-selective late-stage fluorination“ Nature Chem. 2019,
DOI: 10.1038/s41557-019-0353-3.

2.  Site-selective and versatile aromatic C−H functionalization by thianthrenation

F. Berger, M. B. Plutschack, J. Riegger, W. Yu, S. Speicher, M. Ho, N. Frank, T. Ritter “Site-selective and versatile aromatic C−H functionalization by thianthrenation“ Nature 2019, 567, 223–228

DOI: 10.1038/s41586-019-0982-0

3.  Late-Stage Aromatic C–H Oxygenation

J. Börgel, L. Tanwar, F. Berger, T. Ritter “Late-Stage Aromatic C–H Oxygenation“ J. Am. Chem. Soc. 2018, 140, 16026–16031.

DOI: 10.1021/jacs.8b09208

4.  Catalytic dehydrogenative decarboxyolefination of carboxylic acids

X. Sun, J. Chen, T. Ritter “Catalytic dehydrogenative decarboxyolefination of carboxylic acids“ Nat. Chem. 2018, 10, 1229–1233.

DOI: 10.1038/s41557-018-0142-4

5.  Palladium-catalysed electrophilic aromatic C–H fluorination

K. Yamamoto, J. Li, J. A. O. Garber, J. D. Rolfes, G. B. Boursalian, J. C. Borghs, C. Genicot, J. Jacq, M. van Gastel, F. Neese, T. Ritter “Palladium-catalysed electrophilic aromatic C–H fluorination” Nature 2018, 554, 511–514.

DOI: 10.1038/nature25749

6.  Concerted nucleophilic aromatic substitution (CSNAr) with 19F and 18F

C. N. Neumann, J. M. Hooker, T. Ritter “Concerted nucleophilic aromatic substitution (CSNAr) with 19F and 18FNature 2016, 534, 369–373.

DOI: 10.1038/nature17667

7.  A fluoride-derived electrophilic late-stage fluorination reagent for PET imaging

E. Lee, A. S. Kamlet, D. C. Powers, C. N. Neumann, G. B. Boursalian, T. Furuya, D. C. Choi, J. M. Hooker, T. Ritter “A fluoride-derived electrophilic late-stage fluorination reagent for PET imaging” Science 2011, 334, 639–642.

DOI: 10.1126/science.1212625

8.  Deoxyfluorination of phenols

P. Tang, W. Wang, T. Ritter “Deoxyfluorination of phenols” J. Am. Chem. Soc. 2011, 133, 11482‑11484.

DOI: 10.1021/ja2048072

9.  Bimetallic Pd(III) Complexes in Palladium-Catalyzed Carbon–Heteroatom Bond Formation

D. P. Powers, T. Ritter “Bimetallic Pd(III) Complexes in Palladium-Catalyzed Carbon–Heteroatom Bond Formation” Nature Chem. 2009, 1, 302–309.

DOI: 10.1038/nchem.246

10. Carbon–Fluorine Reductive Elimination from a High-Valent Palladium Fluoride

T. Furuya, T. Ritter “Carbon–Fluorine Reductive Elimination from a High-Valent Palladium Fluoride” J. Am. Chem. Soc. 2008, 130, 10060–10061.

DOI: 10.1021/ja803187x

          

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