Charles C. J. Loh

2.1k total citations
45 papers, 1.7k citations indexed

About

Charles C. J. Loh is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Charles C. J. Loh has authored 45 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Organic Chemistry, 18 papers in Molecular Biology and 6 papers in Inorganic Chemistry. Recurrent topics in Charles C. J. Loh's work include Carbohydrate Chemistry and Synthesis (19 papers), Asymmetric Synthesis and Catalysis (18 papers) and Chemical Synthesis and Analysis (14 papers). Charles C. J. Loh is often cited by papers focused on Carbohydrate Chemistry and Synthesis (19 papers), Asymmetric Synthesis and Catalysis (18 papers) and Chemical Synthesis and Analysis (14 papers). Charles C. J. Loh collaborates with scholars based in Germany, Ireland and Canada. Charles C. J. Loh's co-authors include Dieter Enders, Gerhard Raabe, Chunfa Xu, Carsten Strohmann, Suruchi Mahajan, Pankaj Chauhan, André Grossmann, Qijian Ni, Huan Zhang and Carina Merkens and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Charles C. J. Loh

44 papers receiving 1.7k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Charles C. J. Loh Germany 24 1.7k 354 275 74 50 45 1.7k
Balu D. Dherange India 16 1.3k 0.8× 326 0.9× 169 0.6× 127 1.7× 38 0.8× 23 1.5k
Masafumi Ueda Japan 29 2.1k 1.3× 376 1.1× 202 0.7× 163 2.2× 30 0.6× 118 2.2k
Thomas C. Fessard United States 18 1.5k 0.9× 268 0.8× 213 0.8× 182 2.5× 29 0.6× 35 1.7k
Leticia Quintero Mexico 21 1.3k 0.8× 358 1.0× 212 0.8× 64 0.9× 51 1.0× 96 1.5k
Ana M. Martı́n Castro Spain 17 1.3k 0.8× 235 0.7× 211 0.8× 67 0.9× 25 0.5× 39 1.4k
Alexander P. Pulis United Kingdom 27 2.2k 1.3× 180 0.5× 384 1.4× 162 2.2× 26 0.5× 44 2.3k
Uxue Uria Spain 24 1.6k 1.0× 232 0.7× 294 1.1× 83 1.1× 15 0.3× 70 1.7k
Malcolm Spain United Kingdom 23 1.3k 0.8× 252 0.7× 426 1.5× 216 2.9× 25 0.5× 29 1.6k
Gérard Rousseau France 20 964 0.6× 223 0.6× 238 0.9× 72 1.0× 54 1.1× 60 1.1k

Countries citing papers authored by Charles C. J. Loh

Since Specialization
Citations

This map shows the geographic impact of Charles C. J. Loh's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Charles C. J. Loh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Charles C. J. Loh more than expected).

Fields of papers citing papers by Charles C. J. Loh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Charles C. J. Loh. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Charles C. J. Loh. The network helps show where Charles C. J. Loh may publish in the future.

Co-authorship network of co-authors of Charles C. J. Loh

This figure shows the co-authorship network connecting the top 25 collaborators of Charles C. J. Loh. A scholar is included among the top collaborators of Charles C. J. Loh based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Charles C. J. Loh. Charles C. J. Loh is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Loh, Charles C. J.. (2025). Catalytic Strategies for Stereoselective Carbohydrate Synthesis: Emerging Concepts for Accessing Challenging Glycosides. Angewandte Chemie International Edition. 64(42). e202514167–e202514167. 2 indexed citations
2.
Guo, Hao & Charles C. J. Loh. (2025). Noncovalent interactions: An emerging focal point in stereoselective catalytic carbohydrate synthesis. Carbohydrate Research. 552. 109458–109458. 8 indexed citations
3.
Guo, Hao & Charles C. J. Loh. (2025). Enhanced Selectivity of Chalcogen Bonding over Halogen Bonding Catalyzed C ‐glycosylation Through Differentiated Intermediate Activation. Angewandte Chemie International Edition. 65(2). e17553–e17553.
5.
Guo, Hao & Charles C. J. Loh. (2024). Merging radical catalysis and noncovalent stereocontrol concepts to forge native O-glycosidic linkages. Science Bulletin. 69(21). 3308–3310. 3 indexed citations
7.
Strohmann, Carsten, et al.. (2023). Cooperative Bifurcated Chalcogen Bonding and Hydrogen Bonding as Stereocontrolling Elements for Selective Strain-Release Septanosylation. Journal of the American Chemical Society. 145(49). 26611–26622. 41 indexed citations
8.
Demarque, Daniel P., et al.. (2022). A synergistic Rh(I)/organoboron-catalysed site-selective carbohydrate functionalization that involves multiple stereocontrol. Nature Chemistry. 15(3). 424–435. 33 indexed citations
9.
Xu, Chunfa, et al.. (2020). A robust and tunable halogen bond organocatalyzed 2-deoxyglycosylation involving quantum tunneling. Nature Communications. 11(1). 4911–4911. 61 indexed citations
10.
Loh, Charles C. J., Matthias Schmid, Brendan Peters, Xiang Fang, & Mark Lautens. (2016). Exploiting Distal Reactivity of Coumarins: A Rhodium‐Catalyzed Vinylogous Asymmetric Ring‐Opening Reaction. Angewandte Chemie International Edition. 55(14). 4600–4604. 46 indexed citations
11.
Enders, Dieter, et al.. (2015). Organocatalytic Asymmetric Domino Michael/Henry Reaction of Indolin-3-ones with o-Formyl-β-nitrostyrenes. Synthesis. 47(7). 1024–1031. 10 indexed citations
12.
Loh, Charles C. J., Xiang Fang, Brendan Peters, & Mark Lautens. (2015). Benzylic Functionalization of Anthrones via the Asymmetric Ring Opening of Oxabicycles Utilizing a Fourth‐Generation Rhodium Catalytic System. Chemistry - A European Journal. 21(40). 13883–13887. 27 indexed citations
13.
Hack, Daniel, Charles C. J. Loh, Jan Hartmann, Gerhard Raabe, & Dieter Enders. (2014). Merging Gold and Organocatalysis: A Facile Asymmetric Synthesis of Annulated Pyrroles. Chemistry - A European Journal. 20(14). 3917–3921. 25 indexed citations
14.
Ni, Qijian, Huan Zhang, André Grossmann, et al.. (2013). Asymmetric Synthesis of Pyrroloindolones by N‐Heterocyclic Carbene Catalyzed [2+3] Annulation of α‐Chloroaldehydes with Nitrovinylindoles. Angewandte Chemie International Edition. 52(51). 13562–13566. 113 indexed citations
15.
Loh, Charles C. J., Daniel Hack, & Dieter Enders. (2013). Asymmetric domino synthesis of indanes bearing four contiguous stereocentres catalyzed by sub-mol% loadings of a squaramide in minutes. Chemical Communications. 49(87). 10230–10230. 45 indexed citations
16.
Loh, Charles C. J., Iuliana Atodiresei, & Dieter Enders. (2013). Asymmetric Organocatalytic Michael/Henry Domino Reactions through Hydrogen‐Bond Activation: Kinetic Access to Indane Scaffolds Bearing cis‐Vicinal Substituents. Chemistry - A European Journal. 19(33). 10822–10826. 45 indexed citations
17.
Loh, Charles C. J. & Dieter Enders. (2012). Merging Organocatalysis and Gold Catalysis—A Critical Evaluation of the Underlying Concepts. Chemistry - A European Journal. 18(33). 10212–10225. 208 indexed citations
18.
Loh, Charles C. J., Gerhard Raabe, & Dieter Enders. (2012). Enantioselective Synthesis of Tetrahydrocarbazoles through a Michael Addition/Ciamician–Plancher Rearrangement Sequence: Asymmetric Synthesis of a Potent Constrained Analogue of MS‐245. Chemistry - A European Journal. 18(42). 13250–13254. 60 indexed citations
19.
Wang, Chuan, et al.. (2012). Organocatalytic, Asymmetric Synthesis of 3‐Sulfenylated N‐Boc‐Protected Oxindoles. Chemistry - A European Journal. 18(37). 11531–11535. 66 indexed citations
20.
Loh, Charles C. J. & Dieter Enders. (2011). Exploiting the Electrophilic Properties of Indole Intermediates: New Options in Designing Asymmetric Reactions. Angewandte Chemie International Edition. 51(1). 46–48. 137 indexed citations

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