John F. Bower

8.4k total citations · 1 hit paper
134 papers, 7.2k citations indexed

About

John F. Bower is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, John F. Bower has authored 134 papers receiving a total of 7.2k indexed citations (citations by other indexed papers that have themselves been cited), including 124 papers in Organic Chemistry, 41 papers in Inorganic Chemistry and 28 papers in Molecular Biology. Recurrent topics in John F. Bower's work include Catalytic C–H Functionalization Methods (85 papers), Asymmetric Hydrogenation and Catalysis (39 papers) and Catalytic Cross-Coupling Reactions (38 papers). John F. Bower is often cited by papers focused on Catalytic C–H Functionalization Methods (85 papers), Asymmetric Hydrogenation and Catalysis (39 papers) and Catalytic Cross-Coupling Reactions (38 papers). John F. Bower collaborates with scholars based in United Kingdom, United States and Brazil. John F. Bower's co-authors include Michael J. Krische, Steven J. Stanton, Gabriele Fumagalli, Adele Faulkner, Ryan L. Patman, Giacomo E. M. Crisenza, Nicholas J. Race, Megan H. Shaw, James S. Scott and Olga O. Sokolova and has published in prestigious journals such as Chemical Reviews, Proceedings of the National Academy of Sciences and Journal of the American Chemical Society.

In The Last Decade

John F. Bower

126 papers receiving 7.1k citations

Hit Papers

Recent Methodologies That... 2017 2026 2020 2023 2017 250 500 750

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
John F. Bower 6.8k 2.3k 798 344 280 134 7.2k
Li‐Xin Dai 9.6k 1.4× 3.0k 1.3× 1.3k 1.6× 429 1.2× 164 0.6× 201 10.0k
Fuk Yee Kwong 10.1k 1.5× 2.1k 0.9× 1.0k 1.3× 319 0.9× 169 0.6× 193 10.5k
Enrique Gómez‐Bengoa 4.4k 0.6× 1.1k 0.5× 716 0.9× 272 0.8× 171 0.6× 127 4.7k
Naohiko Yoshikai 11.6k 1.7× 3.4k 1.5× 390 0.5× 669 1.9× 318 1.1× 192 11.9k
Marc Taillefer 7.7k 1.1× 1.6k 0.7× 852 1.1× 546 1.6× 239 0.9× 133 8.3k
Arkaitz Correa 5.9k 0.9× 1.4k 0.6× 559 0.7× 311 0.9× 848 3.0× 65 6.5k
Akkattu T. Biju 10.7k 1.6× 1.0k 0.4× 598 0.7× 436 1.3× 305 1.1× 181 10.9k
Gwilherm Evano 7.8k 1.1× 1.2k 0.5× 1.0k 1.3× 560 1.6× 151 0.5× 166 8.4k
Olga Garcı́a Mancheño 4.7k 0.7× 1.1k 0.5× 692 0.9× 193 0.6× 96 0.3× 112 5.0k
Xue‐Long Hou 8.2k 1.2× 3.0k 1.3× 1.3k 1.7× 372 1.1× 145 0.5× 199 8.8k

Countries citing papers authored by John F. Bower

Since Specialization
Citations

This map shows the geographic impact of John F. Bower'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 John F. Bower with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John F. Bower more than expected).

Fields of papers citing papers by John F. Bower

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John F. Bower. 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 John F. Bower. The network helps show where John F. Bower may publish in the future.

Co-authorship network of co-authors of John F. Bower

This figure shows the co-authorship network connecting the top 25 collaborators of John F. Bower. A scholar is included among the top collaborators of John F. Bower 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 John F. Bower. John F. Bower 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.
Chung, Raymond T., Abbas Hassan, Phillippa Cooper, et al.. (2025). Benzamide‐Directed Hydroarylative Cross‐Couplings Using Minimally Activated Alkenes: Enantioselective Synthesis of Tertiary and Quaternary Stereocenters. Angewandte Chemie International Edition. 64(22). e202502569–e202502569. 2 indexed citations
2.
Wang, Yihong, et al.. (2025). β‐Quaternary α‐Amino Acids via Iridium‐Catalyzed Branched and Enantioselective Hydroalkylation of 1,1‐Disubstituted Styrenes. Angewandte Chemie International Edition. 64(26). e202504477–e202504477. 1 indexed citations
3.
García‐Cárceles, Javier, et al.. (2024). A Strategy for the Formal C−N Cross‐Coupling of Tertiary Amines. Angewandte Chemie. 136(50).
4.
Carvalho, Renato L., et al.. (2024). The Synthesis and Reactivity of Naphthoquinonynes. Angewandte Chemie International Edition. 63(18). e202400188–e202400188. 3 indexed citations
5.
García‐Cárceles, Javier, et al.. (2024). A Strategy for the Formal C−N Cross‐Coupling of Tertiary Amines. Angewandte Chemie International Edition. 63(50). e202411555–e202411555. 2 indexed citations
7.
Carvalho, Renato L., Emilay B. T. Diogo, Maria H. Araújo, et al.. (2024). Generation and capture of naphthoquinonynes: a new frontier in the development of trypanocidal quinones via aryne chemistry. RSC Medicinal Chemistry. 16(2). 694–708.
8.
Bower, John F., et al.. (2023). A Stereospecific Alkene 1,2‐Aminofunctionalization Platform for the Assembly of Complex Nitrogen‐Containing Ring Systems. Angewandte Chemie International Edition. 62(16). e202301262–e202301262. 16 indexed citations
9.
Robertson, Craig M., et al.. (2023). Stereospecific Aminative Cyclizations Triggered by Intermolecular Aza‐Prilezhaev Alkene Aziridination. Angewandte Chemie International Edition. 62(48). e202312797–e202312797. 13 indexed citations
11.
Bower, John F., et al.. (2023). A Hemilabile NHC‐Gold Complex and its Application to the Redox Neutral 1,2‐Oxyarylation of Feedstock Alkenes. Angewandte Chemie International Edition. 62(23). e202301526–e202301526. 32 indexed citations
12.
Jardim, Guilherme A. M., et al.. (2022). Looking deep into C–H functionalization: the synthesis and application of cyclopentadienyl and related metal catalysts. Chemical Communications. 58(19). 3101–3121. 25 indexed citations
13.
Young, Tom A., et al.. (2018). Stereospecific Alkene Aziridination Using a Bifunctional Amino-Reagent: An Aza-Prilezhaev Reaction. Journal of the American Chemical Society. 140(51). 17846–17850. 41 indexed citations
14.
Henderson, A. S., John F. Bower, & M. Carmen Galán. (2016). Carbohydrates as enantioinduction components in stereoselective catalysis. Organic & Biomolecular Chemistry. 14(17). 4008–4017. 28 indexed citations
15.
McCreanor, Niall G., Steven J. Stanton, & John F. Bower. (2016). Capture–Collapse Heterocyclization: 1,3-Diazepanes by C–N Reductive Elimination from Rhodacyclopentanones. Journal of the American Chemical Society. 138(36). 11465–11468. 42 indexed citations
16.
Wang, Gang‐Wei, Niall G. McCreanor, Megan H. Shaw, William G. Whittingham, & John F. Bower. (2016). New Initiation Modes for Directed Carbonylative C–C Bond Activation: Rhodium-Catalyzed (3 + 1 + 2) Cycloadditions of Aminomethylcyclopropanes. Journal of the American Chemical Society. 138(41). 13501–13504. 46 indexed citations
17.
Shaw, Megan H., Rosemary A. Croft, William G. Whittingham, & John F. Bower. (2015). Modular Access to Substituted Azocanes via a Rhodium-Catalyzed Cycloaddition–Fragmentation Strategy. Journal of the American Chemical Society. 137(25). 8054–8057. 83 indexed citations
18.
Shaw, Megan H., William G. Whittingham, & John F. Bower. (2015). Directed carbonylative (3+1+2) cycloadditions of amino-substituted cyclopropanes and alkynes: reaction development and increased efficiencies using a cationic rhodium system. Tetrahedron. 72(22). 2731–2741. 29 indexed citations
19.
Crisenza, Giacomo E. M., Olga O. Sokolova, & John F. Bower. (2015). Branch‐Selective Alkene Hydroarylation by Cooperative Destabilization: Iridium‐Catalyzed ortho‐Alkylation of Acetanilides. Angewandte Chemie. 127(49). 15079–15083. 33 indexed citations
20.
Shaw, Megan H., et al.. (2013). Directing Group Enhanced Carbonylative Ring Expansions of Amino-Substituted Cyclopropanes: Rhodium-Catalyzed Multicomponent Synthesis of N-Heterobicyclic Enones. Journal of the American Chemical Society. 135(13). 4992–4995. 116 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

Explore authors with similar magnitude of impact

Rankless by CCL
2026