Michael D. Dowle

796 total citations
22 papers, 530 citations indexed

About

Michael D. Dowle is a scholar working on Organic Chemistry, Molecular Biology and Physiology. According to data from OpenAlex, Michael D. Dowle has authored 22 papers receiving a total of 530 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 7 papers in Molecular Biology and 3 papers in Physiology. Recurrent topics in Michael D. Dowle's work include Synthetic Organic Chemistry Methods (5 papers), Synthesis of heterocyclic compounds (4 papers) and Chemical Synthesis and Analysis (4 papers). Michael D. Dowle is often cited by papers focused on Synthetic Organic Chemistry Methods (5 papers), Synthesis of heterocyclic compounds (4 papers) and Chemical Synthesis and Analysis (4 papers). Michael D. Dowle collaborates with scholars based in United Kingdom. Michael D. Dowle's co-authors include D. I. Davies, Simon J. F. Macdonald, Barry C. Ross, David Middlemiss, D. I. C. SCOPES, Lee A. Harrison, Richard J. Upton, Duncan B. Judd, Stanley M. Roberts and Graham G. A. Inglis and has published in prestigious journals such as Chemical Society Reviews, Journal of Medicinal Chemistry and The Journal of Organic Chemistry.

In The Last Decade

Michael D. Dowle

21 papers receiving 493 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Michael D. Dowle United Kingdom 9 364 177 97 52 34 22 530
Joseph Sisko United States 15 627 1.7× 280 1.6× 56 0.6× 51 1.0× 33 1.0× 27 849
Lisa Frey United States 16 434 1.2× 227 1.3× 138 1.4× 17 0.3× 42 1.2× 25 666
Eiko Imamiya Japan 10 396 1.1× 305 1.7× 27 0.3× 59 1.1× 56 1.6× 16 691
Christopher A. Teleha United States 13 393 1.1× 234 1.3× 56 0.6× 66 1.3× 58 1.7× 32 668
Candido Gude United States 12 487 1.3× 196 1.1× 37 0.4× 23 0.4× 67 2.0× 24 670
Julián Priego Spain 16 701 1.9× 234 1.3× 189 1.9× 15 0.3× 21 0.6× 43 865
Shaoyi Sun China 11 283 0.8× 168 0.9× 46 0.5× 13 0.3× 30 0.9× 19 448
Peter Raddatz Germany 14 239 0.7× 185 1.0× 21 0.2× 41 0.8× 25 0.7× 30 445
Paivi J. Kukkola United States 12 280 0.8× 140 0.8× 34 0.4× 24 0.5× 26 0.8× 17 400
Peter Herold Switzerland 13 572 1.6× 474 2.7× 85 0.9× 150 2.9× 86 2.5× 17 905

Countries citing papers authored by Michael D. Dowle

Since Specialization
Citations

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

Fields of papers citing papers by Michael D. Dowle

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael D. Dowle. 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 Michael D. Dowle. The network helps show where Michael D. Dowle may publish in the future.

Co-authorship network of co-authors of Michael D. Dowle

This figure shows the co-authorship network connecting the top 25 collaborators of Michael D. Dowle. A scholar is included among the top collaborators of Michael D. Dowle 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 Michael D. Dowle. Michael D. Dowle 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.
Dowle, Michael D., et al.. (2005). A stereocontrolled route to protected isocyanates from alcohols. Tetrahedron. 61(8). 2141–2148. 3 indexed citations
2.
Wood, Mark E., et al.. (2003). Synthetic and structural studies on 1,2,4-dithiazolidine-3,5-dione derivatives. Organic & Biomolecular Chemistry. 1(17). 3015–3015. 8 indexed citations
3.
Macdonald, Simon J. F., Michael D. Dowle, Lee A. Harrison, et al.. (2002). Discovery of Further Pyrrolidine trans-Lactams as Inhibitors of Human Neutrophil Elastase (HNE) with Potential as Development Candidates and the Crystal Structure of HNE Complexed with an Inhibitor (GW475151). Journal of Medicinal Chemistry. 45(18). 3878–3890. 48 indexed citations
4.
Macdonald, Simon J. F., et al.. (2002). Syntheses of templates derived from pyrrolidine trans -lactams as potential serine protease inhibitors. Tetrahedron Letters. 43(29). 5057–5060. 4 indexed citations
5.
Wood, Mark E., et al.. (2002). 1,2,4-Dithiazolidine-3,5-dione as an isocyanate equivalent in the Mitsunobu reaction. Journal of the Chemical Society Perkin Transactions 1. 2046–2047. 5 indexed citations
6.
Macdonald, Simon J. F., Geoffrey D. Clarke, Michael D. Dowle, et al.. (1999). A Flexible, Practical, and Stereoselective Synthesis of Enantiomerically Pure trans-5-Oxohexahydropyrrolo[3,2-b]pyrroles (Pyrrolidine-trans-lactams), a New Class of Serine Protease Inhibitors, Using Acyliminium Methodology. The Journal of Organic Chemistry. 64(14). 5166–5175. 31 indexed citations
7.
Dowle, Michael D. & Peter D. Howes. (1998). Recent advances in sialidase inhibitors. Expert Opinion on Therapeutic Patents. 8(11). 1461–1478. 3 indexed citations
8.
Macdonald, Simon J. F., David J. Belton, M. Anson, et al.. (1998). Syntheses of trans-5- Oxo-hexahydro-pyrrolo[3,2-b]pyrroles and trans-5-Oxo-hexahydro-furo[3,2-b]pyrroles (Pyrrolidine trans-Lactams and trans-Lactones):  New Pharmacophores for Elastase Inhibition. Journal of Medicinal Chemistry. 41(21). 3919–3922. 36 indexed citations
9.
Macdonald, Simon J. F., et al.. (1998). A stereoselective synthesis via a 5-exo-trig cyclisation of trans-2-oxohexahydro-2H-furo[3,2-b]pyrroles (pyrrolidine-trans-lactones)—potent, novel elastase inhibitors. Journal of the Chemical Society Perkin Transactions 1. 3931–3936. 9 indexed citations
10.
Macdonald, Simon J. F., et al.. (1998). Synthesis of (+/-)-Oxohexahydrofuro[3,2-b]pyrroles (Pyrrolidine-trans-lactones) via a Reduction-Alkylation Protocol. Synlett. 1998(12). 1378–1380. 6 indexed citations
11.
Macdonald, Simon J. F., et al.. (1998). Synthesis of (+/-)-Oxohexahydrofuro[3,2-b]pyrroles (Pyrrolidine-trans-lactones) Using Acyl-Iminium Chemistry. Synlett. 1998(12). 1375–1377. 7 indexed citations
12.
Judd, Duncan B., Michael D. Dowle, David Middlemiss, et al.. (1994). Bromobenzofuran-Based Non-peptide Antagonists of Angiotensin II: GR138950, a Potent Antihypertensive Agent with High Oral Bioavailability. Journal of Medicinal Chemistry. 37(19). 3108–3120. 33 indexed citations
13.
Middlemiss, David, Steve P. Watson, Barry C. Ross, et al.. (1993). Benzofuran based angiotensi II antagonists related to GR117289: Part II; amino acid amides. Bioorganic & Medicinal Chemistry Letters. 3(10). 2043–2046. 3 indexed citations
14.
Robertson, Mark J., Jen Barnes, G.M. Drew, et al.. (1992). Pharmacological profile of GR117289 in vitro: a novel, potent and specific non‐peptide angiotensin AT1 receptor antagonist. British Journal of Pharmacology. 107(4). 1173–1180. 66 indexed citations
15.
Dowle, Michael D., et al.. (1983). A Convenient Synthesis of Mannich Bases of Thiophene and Substituted Thiophenes. Synthesis. 1983(1). 73–75. 16 indexed citations
16.
Davies, D. I., et al.. (1979). Bromolactones from 2-Norbornene-5-endo-acetic Acid. Synthesis. 1979(12). 990–992. 5 indexed citations
17.
Dowle, Michael D. & D. I. Davies. (1979). Synthesis and synthetic utility of halolactones. Chemical Society Reviews. 8(2). 171–171. 203 indexed citations
18.
Davies, D. I. & Michael D. Dowle. (1978). The acid-catalysed lactonisation of the norborn-5-en-2-ylacetic acids. Journal of the Chemical Society Perkin Transactions 1. 227–227.
19.
Dowle, Michael D.. (1977). New method for converting thioamides into nitriles: use of diethyl azodicarboxylate and triphenylphosphine. Journal of the Chemical Society Chemical Communications. 220–220. 5 indexed citations
20.
Davies, D. I. & Michael D. Dowle. (1976). The iodo-lactones derived from norborn-5-en-2-endo-yl-acetic acid and -propionic acid. Journal of the Chemical Society Perkin Transactions 1. 2267–2267. 8 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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