Thomas M. Razler

758 total citations
19 papers, 545 citations indexed

About

Thomas M. Razler is a scholar working on Organic Chemistry, Biotechnology and Molecular Biology. According to data from OpenAlex, Thomas M. Razler has authored 19 papers receiving a total of 545 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Organic Chemistry, 5 papers in Biotechnology and 4 papers in Molecular Biology. Recurrent topics in Thomas M. Razler's work include Synthetic Organic Chemistry Methods (10 papers), Marine Sponges and Natural Products (5 papers) and Asymmetric Synthesis and Catalysis (4 papers). Thomas M. Razler is often cited by papers focused on Synthetic Organic Chemistry Methods (10 papers), Marine Sponges and Natural Products (5 papers) and Asymmetric Synthesis and Catalysis (4 papers). Thomas M. Razler collaborates with scholars based in United States, France and Germany. Thomas M. Razler's co-authors include Amos B. Smith, Richard J. Fox, Yi Hsiao, George R. Pettit, Tomoyasu Hirose, Tomoyasu Ishikawa, Yuping Qiu, Paul Jackson, Yuemei Zhang and Eric M. Simmons and has published in prestigious journals such as Journal of the American Chemical Society, Accounts of Chemical Research and The Journal of Organic Chemistry.

In The Last Decade

Thomas M. Razler

19 papers receiving 530 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Thomas M. Razler United States 11 494 107 79 66 58 19 545
Daniel D. Caspi United States 8 402 0.8× 94 0.9× 96 1.2× 52 0.8× 30 0.5× 14 469
Marie‐Isabelle Lannou France 12 402 0.8× 103 1.0× 42 0.5× 71 1.1× 60 1.0× 31 442
Michael C. Hillier United States 14 409 0.8× 199 1.9× 53 0.7× 56 0.8× 39 0.7× 21 521
Cedric L. Hugelshofer Germany 14 387 0.8× 163 1.5× 42 0.5× 89 1.3× 84 1.4× 21 531
Alois Fuerstner Germany 9 631 1.3× 131 1.2× 87 1.1× 67 1.0× 70 1.2× 35 694
Achim Lenzen Germany 10 635 1.3× 190 1.8× 141 1.8× 41 0.6× 89 1.5× 14 711
Keiji Nakano Japan 16 715 1.4× 243 2.3× 154 1.9× 53 0.8× 61 1.1× 51 784
Shaojing Hu Canada 11 393 0.8× 77 0.7× 62 0.8× 32 0.5× 43 0.7× 15 458
Stephen E. Shanahan United Kingdom 8 307 0.6× 114 1.1× 105 1.3× 22 0.3× 43 0.7× 13 422

Countries citing papers authored by Thomas M. Razler

Since Specialization
Citations

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

Fields of papers citing papers by Thomas M. Razler

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Thomas M. Razler. 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 Thomas M. Razler. The network helps show where Thomas M. Razler may publish in the future.

Co-authorship network of co-authors of Thomas M. Razler

This figure shows the co-authorship network connecting the top 25 collaborators of Thomas M. Razler. A scholar is included among the top collaborators of Thomas M. Razler 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 Thomas M. Razler. Thomas M. Razler is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Tábora, José E., Eric C. Huang, Steven R. Wisniewski, et al.. (2019). Development and Implementation of a Quality Control Strategy for an Atropisomer Impurity Grounded in a Risk-Based Probabilistic Design Space. Organic Process Research & Development. 23(2). 211–219. 6 indexed citations
2.
Wisniewski, Steven R., et al.. (2019). Systematic Optimization of a Robust Telescoped Process for a BTK Inhibitor with Atropisomer Control by High-Throughput Experimentation, Design of Experiments, and Linear Regression. Organic Process Research & Development. 23(6). 1143–1151. 7 indexed citations
3.
Wisniewski, Steven R., Ronald Carrasquillo‐Flores, Antonio Ramı́rez, et al.. (2018). Adventures in Atropisomerism: Development of a Robust, Diastereoselective, Lithium-Catalyzed Atropisomer-Forming Active Pharmaceutical Ingredient Step. Organic Process Research & Development. 22(10). 1426–1431. 8 indexed citations
4.
Beutner, Gregory L., Yi Hsiao, Thomas M. Razler, Eric M. Simmons, & William C. Wertjes. (2017). Nickel-Catalyzed Synthesis of Quinazolinediones. Organic Letters. 19(5). 1052–1055. 40 indexed citations
5.
Gao, Qi, et al.. (2017). From Drying Kinetics, Solvate Structure, Particle Morphology, and Modeling to Optimal Drying Protocol. Organic Process Research & Development. 21(10). 1509–1520. 8 indexed citations
6.
Simmons, Eric M., Boguslaw Mudryk, Andrew G. Lee, et al.. (2017). Development of a Kilogram-Scale Process for the Enantioselective Synthesis of 3-Isopropenyl-cyclohexan-1-one via Rh/DTBM-SEGPHOS-Catalyzed Asymmetric Hayashi Addition Enabled by 1,3-Diol Additives. Organic Process Research & Development. 21(10). 1659–1667. 19 indexed citations
7.
Conlon, David A., Kenneth J. Natalie, Thomas M. Razler, et al.. (2016). Development of a Practical Synthesis of Functionalized Azaxanthene-Derived Nonsteroidal Glucocorticoid Receptor Modulators. Organic Process Research & Development. 20(5). 921–933. 5 indexed citations
8.
Ji, Yining, R. Erik Plata, Christopher S. Regens, et al.. (2015). Mono-Oxidation of Bidentate Bis-phosphines in Catalyst Activation: Kinetic and Mechanistic Studies of a Pd/Xantphos-Catalyzed C–H Functionalization. Journal of the American Chemical Society. 137(41). 13272–13281. 103 indexed citations
9.
Huang, Yande, et al.. (2012). Degradation Kinetics and Mechanism of an Oxadiazole Derivative, Design of a Stable Drug Product for BMS-708163, a γ-Secretase Inhibitor Drug Candidate. Journal of Pharmaceutical Sciences. 101(9). 3124–3133. 5 indexed citations
10.
Smith, Amos B., Anne‐Marie L. Hogan, Zhuqing Liu, et al.. (2011). Phorboxazole synthetic studies: design, synthesis and biological evaluation of phorboxazole A and hemi-phorboxazole A related analogues. Tetrahedron. 67(27-28). 5069–5078. 6 indexed citations
11.
Zhu, Jason, et al.. (2011). A Robust Three-Step Telescoped Synthesis of Electron- Deficient Amide Substituted Arylboronic Acids. Organic Process Research & Development. 15(2). 438–442. 8 indexed citations
12.
Razler, Thomas M., et al.. (2008). A Preparatively Convenient Ligand-Free Catalytic PEG 2000 Suzuki−Miyaura Coupling. The Journal of Organic Chemistry. 74(3). 1381–1384. 62 indexed citations
13.
Smith, Amos B., et al.. (2008). A Second-Generation Total Synthesis of (+)-Phorboxazole A. The Journal of Organic Chemistry. 73(4). 1192–1200. 33 indexed citations
14.
15.
16.
Smith, Amos B., et al.. (2006). Design and Synthesis of a Potent Phorboxazole C(11−15) Acetal Analogue. Organic Letters. 8(4). 797–799. 18 indexed citations
17.
Smith, Amos B., et al.. (2005). (+)-Phorboxazole A Synthetic Studies. A Highly Convergent, Second Generation Total Synthesis of (+)-Phorboxazole A. Organic Letters. 7(20). 4399–4402. 36 indexed citations
18.
Smith, Amos B., Thomas M. Razler, George R. Pettit, & Jean‐Charles Chapuis. (2005). (+)-Phorboxazole A Synthetic Studies. Identification of a Series of Highly Cytotoxic C(45−46) Analogues. Organic Letters. 7(20). 4403–4406. 23 indexed citations
19.
Zhang, Yuemei, Thomas M. Razler, & Paul Jackson. (2002). Synthesis of pyrimido[4,5-b]indoles and benzo[4,5]furo[2,3-d]pyrimidines via palladium-catalyzed intramolecular arylation. Tetrahedron Letters. 43(46). 8235–8239. 35 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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