Matthew L. Maddess

1.1k total citations
31 papers, 375 citations indexed

About

Matthew L. Maddess is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Matthew L. Maddess has authored 31 papers receiving a total of 375 indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Organic Chemistry, 13 papers in Molecular Biology and 7 papers in Inorganic Chemistry. Recurrent topics in Matthew L. Maddess's work include Synthetic Organic Chemistry Methods (13 papers), Chemical Synthesis and Analysis (8 papers) and Asymmetric Synthesis and Catalysis (6 papers). Matthew L. Maddess is often cited by papers focused on Synthetic Organic Chemistry Methods (13 papers), Chemical Synthesis and Analysis (8 papers) and Asymmetric Synthesis and Catalysis (6 papers). Matthew L. Maddess collaborates with scholars based in United States, Canada and United Kingdom. Matthew L. Maddess's co-authors include Mark Lautens, J. Adam McCubbin, Stéphane G. Ouellet, Effiette L. O. Sauer, Steven V. Ley, Christopher D. Spilling, Hidenori Watanabe, James S. Scott, Paul E. Brennan and Letian Wang and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

Matthew L. Maddess

29 papers receiving 368 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Matthew L. Maddess United States 12 250 119 48 41 38 31 375
David McLeod Canada 15 474 1.9× 118 1.0× 11 0.2× 39 1.0× 35 0.9× 28 590
Deepti Goyal India 12 235 0.9× 152 1.3× 28 0.6× 30 0.7× 29 0.8× 20 369
Pierrik Lassalas France 7 309 1.2× 158 1.3× 34 0.7× 34 0.8× 11 0.3× 11 477
David A. Favor United States 11 300 1.2× 140 1.2× 12 0.3× 26 0.6× 21 0.6× 17 388
Ngiap‐Kie Lim United States 12 321 1.3× 94 0.8× 26 0.5× 18 0.4× 39 1.0× 27 399
Teresa A. Palazzo United States 15 520 2.1× 117 1.0× 14 0.3× 21 0.5× 35 0.9× 23 612
Johanne Renaud Switzerland 12 309 1.2× 221 1.9× 65 1.4× 27 0.7× 19 0.5× 17 512
Iwona Wrona United States 10 276 1.1× 112 0.9× 12 0.3× 66 1.6× 32 0.8× 13 391
Martin P. Allen United States 10 276 1.1× 254 2.1× 45 0.9× 61 1.5× 23 0.6× 14 458
Sergey E. Pipko Ukraine 13 307 1.2× 125 1.1× 21 0.4× 28 0.7× 28 0.7× 25 371

Countries citing papers authored by Matthew L. Maddess

Since Specialization
Citations

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

Fields of papers citing papers by Matthew L. Maddess

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew L. Maddess. 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 Matthew L. Maddess. The network helps show where Matthew L. Maddess may publish in the future.

Co-authorship network of co-authors of Matthew L. Maddess

This figure shows the co-authorship network connecting the top 25 collaborators of Matthew L. Maddess. A scholar is included among the top collaborators of Matthew L. Maddess 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 Matthew L. Maddess. Matthew L. Maddess 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.
Candito, David A., Ping Liu, Michael J. Ardolino, et al.. (2025). A Concise Synthesis of a Key Azabicyclo[2.1.1]hexane Building Block for N-Heteroaryl Indazole LRRK2 Kinase Inhibitors. Synlett. 36(16). 2661–2665. 1 indexed citations
2.
Maddess, Matthew L., Ed Cleator, Mariko Morimoto, et al.. (2024). Process Development of a Tricyclic Diazepine-Based IDH1 Mutant Inhibitor. Organic Process Research & Development. 28(6). 2343–2354. 2 indexed citations
3.
Petrone, David A., Damien Valette, Justin A. Newman, et al.. (2024). HTE-Enabled Development of an Ene-Reductase-Catalyzed Desymmetrization: Remote Control of All-Carbon Quaternary γ-Centers. Organic Letters. 26(51). 11212–11217. 1 indexed citations
4.
Patel, Chirag, Andrew J. Neel, Barbara Pio, et al.. (2023). A General Strategy for N-(Hetero)arylpiperidine Synthesis Using Zincke Imine Intermediates. Journal of the American Chemical Society. 146(1). 936–945. 12 indexed citations
5.
Maddess, Matthew L., David L. Sloman, Xiaoshen Ma, et al.. (2023). Abstract B074: Discovery of MK-1084, a low dose selective clinical stage KRAS G12C inhibitor. Molecular Cancer Therapeutics. 22(12_Supplement). B074–B074. 1 indexed citations
6.
Maddess, Matthew L., Ed Cleator, Mariko Morimoto, et al.. (2021). Development of a Stereoselective Synthesis of (1R,4R)- and (1S,4S)-2-Oxa-5-azabicyclo[2.2.2]octane. Organic Process Research & Development. 26(3). 640–647. 6 indexed citations
7.
Bryce, Dianne K., Paul J. Ciaccio, Laxminarayan G. Hegde, et al.. (2021). Characterization of the Onset, Progression, and Reversibility of Morphological Changes in Mouse Lung after Pharmacological Inhibition of Leucine-Rich Kinase 2 Kinase Activity. Journal of Pharmacology and Experimental Therapeutics. 377(1). 11–19. 14 indexed citations
8.
Zárate, Cayetana, Michael J. Ardolino, Gregori J. Morriello, et al.. (2020). Development of Scalable Routes to 1-Bicyclo[1.1.1]pentylpyrazoles. Organic Process Research & Development. 25(3). 642–647. 27 indexed citations
9.
Martinot, Theodore A., Michael J. Ardolino, Lu Chen, et al.. (2019). Process Safety Considerations for the Supply of a High-Energy Oxadiazole IDO1-Selective Inhibitor. Organic Process Research & Development. 23(6). 1178–1190. 3 indexed citations
10.
Maddess, Matthew L. & Chaomin Li. (2018). Metal Catalyzed Synthesis of Dihydropyridobenzodiazepines. Organometallics. 38(1). 81–84. 4 indexed citations
11.
Sheridan, Robert P., Nicolas F. Zorn, Edward C. Sherer, et al.. (2014). Modeling a Crowdsourced Definition of Molecular Complexity. Journal of Chemical Information and Modeling. 54(6). 1604–1616. 53 indexed citations
12.
Maddess, Matthew L., Jeremy P. Scott, Carl A. Baxter, et al.. (2014). Enantioselective Synthesis of a Highly Substituted Tetrahydrofluorene Derivative as a Potent and Selective Estrogen Receptor Beta Agonist. Organic Process Research & Development. 18(4). 528–538. 11 indexed citations
13.
14.
Lautens, Mark, J. Adam McCubbin, & Matthew L. Maddess. (2011). Enantioselective Allylation and Crotylation of in situ Generated β,γ-Unsaturated Aldehydes. Synlett. 2011(19). 2857–2861.
15.
Maddess, Matthew L., et al.. (2008). Total synthesis studies on macrocyclic pipecolic acid natural products: FK506, the antascomicins and rapamycin. Birkhäuser Basel eBooks. 66. 13–186. 8 indexed citations
16.
Maddess, Matthew L., E. Mainetti, Youssef Harrak, et al.. (2007). Preparation of fused polycyclic vinylcyclopropanes via radical cascade reactions. Chemical Communications. 936–936. 8 indexed citations
17.
Wang, Letian, Matthew L. Maddess, & Mark Lautens. (2007). Convenient Access to Functionalized Vinylcyclopentenols from Alkynyloxiranes. The Journal of Organic Chemistry. 72(5). 1822–1825. 22 indexed citations
18.
McCubbin, J. Adam, Matthew L. Maddess, & Mark Lautens. (2006). Total Synthesis of Cryptophycin Analogues via a Scaffold Approach. Organic Letters. 8(14). 2993–2996. 36 indexed citations
19.
Maddess, Matthew L., Hidenori Watanabe, Paul E. Brennan, et al.. (2006). Total Synthesis of Rapamycin. Angewandte Chemie International Edition. 46(4). 591–597. 41 indexed citations
20.
Maddess, Matthew L. & Mark Lautens. (2005). Preparation of Homoallylic Homopropargylic Alcohols from 2-Vinyloxiranes. Organic Letters. 7(16). 3557–3560. 18 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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