Edward C. Lawson

752 total citations
18 papers, 487 citations indexed

About

Edward C. Lawson is a scholar working on Organic Chemistry, Molecular Biology and Surgery. According to data from OpenAlex, Edward C. Lawson has authored 18 papers receiving a total of 487 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Organic Chemistry, 7 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Edward C. Lawson's work include Chemical Synthesis and Analysis (5 papers), Asymmetric Synthesis and Catalysis (5 papers) and Synthesis and Catalytic Reactions (4 papers). Edward C. Lawson is often cited by papers focused on Chemical Synthesis and Analysis (5 papers), Asymmetric Synthesis and Catalysis (5 papers) and Synthesis and Catalytic Reactions (4 papers). Edward C. Lawson collaborates with scholars based in United States, United Kingdom and South Korea. Edward C. Lawson's co-authors include James M. Takacs, Bruce E. Maryanoff, William A. Kinney, Bruce P. Damiano, William J. Hoekstra, Shyamali Ghosh, Diane K. Luci, Charles E. Smith, Lisa Minor and Yuanping Wang and has published in prestigious journals such as Journal of the American Chemical Society, Advanced Functional Materials and Journal of Medicinal Chemistry.

In The Last Decade

Edward C. Lawson

18 papers receiving 478 citations

Peers

Edward C. Lawson

BIOMA

PHARM

Thomas Neubauer Netherlands

Cheng Lü China

Hongrui Song China

Andrew R. Gibbs United States

Heng Xu China

Bao Hu China

Craig S. Harris France

Steven R. Woulfe United States

Abdolhossein Zarrin Iran

Thomas Neubauer Netherlands

Edward C. Lawson

225 ×0.7

112 ×0.8

31 ×0.6

62 ×1.5

BIOMA

28 ×0.7

PHARM

Citations per year, relative to Edward C. Lawson Edward C. Lawson (= 1×) peers Thomas Neubauer

Countries citing papers authored by Edward C. Lawson

Since Specialization

Citations

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

Fields of papers citing papers by Edward C. Lawson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Edward C. Lawson. 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 Edward C. Lawson. The network helps show where Edward C. Lawson may publish in the future.

Co-authorship network of co-authors of Edward C. Lawson

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

All Works

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18 of 18 papers shown

Lawson, Edward C., et al.. (2020). Tandem Suzuki Coupling/Intramolecular Oxetane Ring Opening to Form Polycyclic Ring Systems. Organic Letters. 22(15). 5828–5832. 15 indexed citations

Choi, Ki Young, Santiago Correa, Jouha Min, et al.. (2019). Binary Targeting of siRNA to Hematologic Cancer Cells In Vivo Using Layer‐by‐Layer Nanoparticles. Advanced Functional Materials. 29(20). 94 indexed citations

Lawson, Edward C., et al.. (2019). Mild Intramolecular Ring Opening of Oxetanes. Organic Letters. 21(23). 9642–9645. 20 indexed citations

Luci, Diane K., Edward C. Lawson, Shyamali Ghosh, et al.. (2009). Generation of novel, potent urotensin-II receptor antagonists by alkylation–cyclization of isoindolinone C3-carbanions. Tetrahedron Letters. 50(35). 4958–4961. 30 indexed citations

Lawson, Edward C., Diane K. Luci, Shyamali Ghosh, et al.. (2009). Nonpeptide Urotensin-II Receptor Antagonists: A New Ligand Class Based on Piperazino-Phthalimide and Piperazino-Isoindolinone Subunits. Journal of Medicinal Chemistry. 52(23). 7432–7445. 69 indexed citations

Luci, Diane K., Shyamali Ghosh, Charles E. Smith, et al.. (2007). Phenylpiperidine-benzoxazinones as urotensin-II receptor antagonists: Synthesis, SAR, and in vivo assessment. Bioorganic & Medicinal Chemistry Letters. 17(23). 6489–6492. 14 indexed citations

Lawson, Edward C., Rosemary J. Santulli, Alexey B. Dyatkin, et al.. (2006). Selection of a 2-azabicyclo[2.2.2]octane-based α4β1 integrin antagonist as an inhaled anti-asthmatic agent. Bioorganic & Medicinal Chemistry. 14(12). 4208–4216. 10 indexed citations

Ghosh, Shyamali, William A. Kinney, Diane A. Gauthier, et al.. (2006). Convenient preparation of aryl-substituted nortropanes by SuzukiMiyaura methodology. Canadian Journal of Chemistry. 84(4). 555–560. 8 indexed citations

Lawson, Edward C., et al.. (2005). Synthesis and Biological Evaluation of 1,2,4-Triazolo[2,3-a]pyrrole Derivatives as Alpha-4 ( α4) Integrin Antagonists. Letters in Drug Design & Discovery. 2(8). 601–605. 5 indexed citations

10.

Lawson, Edward C., William A. Kinney, Michael J. Costanzo, et al.. (2004). Structure-Function Study of Quinazolinone-Based Vitronectin Receptor (αVβ3) Antagonists: Computer-Assisted Analysis of Ligand-Receptor Interactions. Letters in Drug Design & Discovery. 1(1). 14–18. 8 indexed citations

11.

Lawson, Edward C., William A. Kinney, Diane K. Luci, et al.. (2002). The Heck reaction with unprotected allylic amidines and guanidines. Tetrahedron Letters. 43(11). 1951–1953. 5 indexed citations

12.

Lawson, Edward C., William J. Hoekstra, Marylyn M. Addo, et al.. (2001). 1,2,4-Triazolo[3,4-a]pyridine as a novel, constrained template for fibrinogen receptor (GPIIb/IIIa) antagonists. Bioorganic & Medicinal Chemistry Letters. 11(19). 2619–2622. 47 indexed citations

13.

Lawson, Edward C., Bruce E. Maryanoff, & William J. Hoekstra. (2000). Synthesis of triazolopyridines as conformationally constrained tertiary amides. Tetrahedron Letters. 41(23). 4533–4536. 21 indexed citations

14.

Lawson, Edward C., Han‐Cheng Zhang, & Bruce E. Maryanoff. (1999). Remote stereocontrol in acyclic systems. Hydride addition to 1,5- and 1,6-hydroxy ketones mediated by metal chelation. Tetrahedron Letters. 40(4). 593–596. 5 indexed citations

15.

Zhang, Han‐Cheng, Bruce D. Harris, Michael J. Costanzo, et al.. (1998). Stereocontrol between Remote Atom Centers in Acyclic Substrates. Anti Addition of Hydride to 1,5-, 1,6-, and 1,7-Hydroxy Ketones. The Journal of Organic Chemistry. 63(22). 7964–7981. 14 indexed citations

16.

Takacs, James M., et al.. (1997). Enantioselective Diels-Alder reactions: room temperature bis(oxazoline)-zinc, -magnesium, and -copper triflate catalysts. Tetrahedron Asymmetry. 8(18). 3073–3078. 41 indexed citations

17.

Takacs, James M., et al.. (1997). On the Nature of the Catalytic Palladium-Mediated Elimination of Allylic Carbonates and Acetates To Form 1,3-Dienes. Journal of the American Chemical Society. 119(25). 5956–5957. 75 indexed citations

18.

Takacs, James M. & Edward C. Lawson. (1994). Catalytic Rhodium-Mediated Tetraene Carbocyclizations. Organometallics. 13(12). 4787–4793. 6 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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