Stephen A. Hermitage

894 total citations
45 papers, 729 citations indexed

About

Stephen A. Hermitage is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Stephen A. Hermitage has authored 45 papers receiving a total of 729 indexed citations (citations by other indexed papers that have themselves been cited), including 30 papers in Organic Chemistry, 9 papers in Inorganic Chemistry and 8 papers in Molecular Biology. Recurrent topics in Stephen A. Hermitage's work include Asymmetric Synthesis and Catalysis (17 papers), Oxidative Organic Chemistry Reactions (9 papers) and Synthesis and Catalytic Reactions (8 papers). Stephen A. Hermitage is often cited by papers focused on Asymmetric Synthesis and Catalysis (17 papers), Oxidative Organic Chemistry Reactions (9 papers) and Synthesis and Catalytic Reactions (8 papers). Stephen A. Hermitage collaborates with scholars based in United Kingdom, Italy and Ireland. Stephen A. Hermitage's co-authors include D. Christopher Braddock, Andrew J. P. White, Andrew Whiting, Mark G. Moloney, Joanna M. Redmond, Stanley M. Roberts, Judith A. K. Howard, Robin G. Pritchard, Michael R. Probert and Catherine Davies and has published in prestigious journals such as Chemical Communications, Tetrahedron and Tetrahedron Letters.

In The Last Decade

Stephen A. Hermitage

43 papers receiving 714 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephen A. Hermitage United Kingdom 16 672 227 141 42 39 45 729
Kazuo Yanada Japan 15 716 1.1× 151 0.7× 146 1.0× 50 1.2× 15 0.4× 44 820
Thierry Schlama France 13 396 0.6× 144 0.6× 172 1.2× 21 0.5× 27 0.7× 28 547
Heinrich Becker United States 12 592 0.9× 145 0.6× 188 1.3× 32 0.8× 54 1.4× 17 724
Gustav Dickmeiss Denmark 14 1.4k 2.1× 311 1.4× 234 1.7× 29 0.7× 24 0.6× 16 1.5k
Wendy S. Jen United States 4 751 1.1× 171 0.8× 152 1.1× 12 0.3× 38 1.0× 4 803
Vishnumaya Bisai India 15 926 1.4× 181 0.8× 193 1.4× 35 0.8× 21 0.5× 28 985
Paraselli Bheema Rao United States 12 731 1.1× 110 0.5× 149 1.1× 53 1.3× 30 0.8× 16 790
Pompiliu S. Aburel Denmark 11 903 1.3× 270 1.2× 222 1.6× 20 0.5× 21 0.5× 14 921
Nils Rackelmann Germany 9 740 1.1× 113 0.5× 148 1.0× 25 0.6× 21 0.5× 11 827
Björn C.G. Söderberg United States 24 1.4k 2.1× 302 1.3× 191 1.4× 92 2.2× 22 0.6× 70 1.5k

Countries citing papers authored by Stephen A. Hermitage

Since Specialization
Citations

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

Fields of papers citing papers by Stephen A. Hermitage

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen A. Hermitage. 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 Stephen A. Hermitage. The network helps show where Stephen A. Hermitage may publish in the future.

Co-authorship network of co-authors of Stephen A. Hermitage

This figure shows the co-authorship network connecting the top 25 collaborators of Stephen A. Hermitage. A scholar is included among the top collaborators of Stephen A. Hermitage 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 Stephen A. Hermitage. Stephen A. Hermitage 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.
Urquhart, Michael W., Ben Bardsley, Andrew J. Edwards, et al.. (2018). Managing emerging mutagenicity risks: Late stage mutagenic impurity control within the atovaquone second generation synthesis. Regulatory Toxicology and Pharmacology. 99. 22–32. 4 indexed citations
2.
Braddock, D. Christopher, et al.. (2009). The generation and trapping of enantiopure bromonium ions. Chemical Communications. 1082–1082. 30 indexed citations
3.
Rassias, Gerasimos & Stephen A. Hermitage. (2009). Controlling thiiranium intermediates—a new route to an iNOS inhibitor. Tetrahedron Letters. 50(40). 5565–5568. 1 indexed citations
4.
Braddock, D. Christopher, et al.. (2007). Amidines as potent nucleophilic organocatalysts for the transfer of electrophilic bromine from N-bromosuccinimide to alkenes. Tetrahedron Letters. 48(34). 5948–5952. 52 indexed citations
5.
Braddock, D. Christopher, et al.. (2006). Ortho-substituted iodobenzenes as novel organocatalysts for bromination of alkenes. Chemical Communications. 2483–2483. 70 indexed citations
6.
Bari, Lorenzo Di, et al.. (2005). Absolute stereochemistry assignment of N‐phosphorylimine‐derived aza‐Diels‐Alder adducts with TDDFT CD calculations. Chirality. 17(6). 323–331. 23 indexed citations
7.
Hermitage, Stephen A., et al.. (2004). Mechanistic studies on the formal aza-Diels–Alder reactions of N-aryl imines: evidence for the non-concertedness under Lewis-acid catalysed conditions. Organic & Biomolecular Chemistry. 2(17). 2451–2460. 65 indexed citations
8.
Brewster, Andrew G., et al.. (2004). Enantiopure bicyclic piperidinones: stereoselectivity in lactam enolate alkylations. Organic & Biomolecular Chemistry. 2(7). 1031–1043. 11 indexed citations
9.
Braddock, D. Christopher, et al.. (2004). An asymmetric synthesis of enantiopure chair and twist trans-cyclooctene isomers. Tetrahedron Asymmetry. 15(19). 3123–3129. 25 indexed citations
10.
Bari, Lorenzo Di, Stéphane Guillarme, Stephen A. Hermitage, et al.. (2004). Lewis Acid Catalyzed Aza‐Diels—Alder versus Mannich Reactions of N‐Diethyl Phosphoryl Imino Dienophiles with Oxygenated Dienes and Application of a Chiral Lewis Acid.. ChemInform. 35(30). 1 indexed citations
11.
Whiting, Andrew, Lorenzo Di Bari, Stéphane Guillarme, et al.. (2004). Lewis Acid-catalysed Aza-Diels-AlderversusMannich Reactions ofN-Diethyl Phosphoryl Imino Dienophiles with Oxygenated Dienes and Application of a Chiral Lewis Acid. Synlett. 708–710. 1 indexed citations
13.
Laird, Trevor, Stephen A. Hermitage, & Ulf Tilstam. (2003). Some Items of Interest to Process R&D Chemists and Engineers. Organic Process Research & Development. 7(2). 124–134. 1 indexed citations
14.
Laird, Trevor, Stephen A. Hermitage, & Ulf Tilstam. (2002). Some Items of Interest to Process R&D Chemists and Engineers. Organic Process Research & Development. 6(2). 90–97. 1 indexed citations
15.
Reynolds, Dominic J. & Stephen A. Hermitage. (2001). The synthesis of GW710936X to support the development of potent PPARγ agonists. Tetrahedron. 57(36). 7765–7770. 1 indexed citations
16.
Hermitage, Stephen A., et al.. (2000). An Efficient, Practical Approach to the Synthesis of 2,4-Disubstituted Thiazoles and Oxazoles:  Application to the Synthesis of GW475151. Organic Process Research & Development. 5(1). 37–44. 26 indexed citations
17.
Laird, Trevor & Stephen A. Hermitage. (1999). Some Items of Interest to Process R&D Chemists and Engineers as Selected by Trevor Laird and Stephen A. Hermitage. Organic Process Research & Development. 4(1). 2–9. 1 indexed citations
18.
Hermitage, Stephen A., et al.. (1998). Synthesis and biological activity of lactones en route to Altohyrtin A. Bioorganic & Medicinal Chemistry Letters. 8(13). 1635–1638. 6 indexed citations
19.
Hermitage, Stephen A., Stanley M. Roberts, & Daniel J. Watson. (1998). Approaches to the C-24 to C-37 perimeter of altohyrtin A. Tetrahedron Letters. 39(21). 3567–3570. 20 indexed citations
20.
Hermitage, Stephen A. & Mark G. Moloney. (1994). Short approach to functionalised homochiral piperidinones. Tetrahedron Asymmetry. 5(8). 1463–1464. 27 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.

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