Douglas E. Stack

1.5k total citations · 1 hit paper
26 papers, 1.2k citations indexed

About

Douglas E. Stack is a scholar working on Organic Chemistry, Molecular Biology and Genetics. According to data from OpenAlex, Douglas E. Stack has authored 26 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Organic Chemistry, 8 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Douglas E. Stack's work include Estrogen and related hormone effects (8 papers), Asymmetric Synthesis and Catalysis (7 papers) and Synthesis and Biological Evaluation (5 papers). Douglas E. Stack is often cited by papers focused on Estrogen and related hormone effects (8 papers), Asymmetric Synthesis and Catalysis (7 papers) and Synthesis and Biological Evaluation (5 papers). Douglas E. Stack collaborates with scholars based in United States. Douglas E. Stack's co-authors include Ercole L. Cavalieri, Eleanor G. Rogan, Michael L. Gross, Ragulan Ramanathan, Indra Dwivedy, Ronald L. Cerny, Kashinath D. Patil, Sonny L. Johansson, Prabhakar D. Devanesan and Sheila Higginbotham and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and The Journal of Organic Chemistry.

In The Last Decade

Douglas E. Stack

26 papers receiving 1.2k citations

Hit Papers

Molecular origin of cancer: Catechol estrogen-3,4-quinone... 1997 2026 2006 2016 1997 200 400 600

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Douglas E. Stack United States 13 579 546 300 178 139 26 1.2k
R. MCCAGUE United Kingdom 20 564 1.0× 537 1.0× 566 1.9× 230 1.3× 92 0.7× 54 1.4k
Cecil H. Robinson United States 14 432 0.7× 524 1.0× 201 0.7× 92 0.5× 55 0.4× 39 990
Y. R. Santosh Laxmi United States 16 323 0.6× 241 0.4× 225 0.8× 90 0.5× 74 0.5× 31 747
Peter C. Ruenitz United States 17 254 0.4× 340 0.6× 268 0.9× 118 0.7× 35 0.3× 57 811
J. Neville Wright United Kingdom 21 691 1.2× 469 0.9× 117 0.4× 219 1.2× 67 0.5× 43 1.6k
John M. Roman United States 14 403 0.7× 218 0.4× 110 0.4× 170 1.0× 176 1.3× 24 1.1k
Goutam Chowdhury United States 27 852 1.5× 68 0.1× 250 0.8× 168 0.9× 262 1.9× 46 1.4k
M. L. Sá e Melo Portugal 18 501 0.9× 196 0.4× 448 1.5× 70 0.4× 28 0.2× 55 1.1k
David S. Weinstein United States 16 343 0.6× 90 0.2× 362 1.2× 126 0.7× 109 0.8× 34 918
Bryan H. Norman United States 26 549 0.9× 166 0.3× 667 2.2× 292 1.6× 36 0.3× 49 1.4k

Countries citing papers authored by Douglas E. Stack

Since Specialization
Citations

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

Fields of papers citing papers by Douglas E. Stack

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Douglas E. Stack. 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 Douglas E. Stack. The network helps show where Douglas E. Stack may publish in the future.

Co-authorship network of co-authors of Douglas E. Stack

This figure shows the co-authorship network connecting the top 25 collaborators of Douglas E. Stack. A scholar is included among the top collaborators of Douglas E. Stack 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 Douglas E. Stack. Douglas E. Stack 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.
Dong, Yuxiang, Jered C. Garrison, Xiaofang Wang, et al.. (2020). Tricyclic Imidazolidin-4-ones by Witkop Oxidation of Tetrahydro-β-carbolines. The Journal of Organic Chemistry. 85(4). 2846–2853. 8 indexed citations
2.
Wu, Jianbo, Yuxiang Dong, Xiaofang Wang, et al.. (2018). Synthesis of 2-Azaadamantan-6-one: A Missing Isomer. ACS Omega. 3(9). 11362–11367. 5 indexed citations
3.
Dong, Yuxiang, et al.. (2017). One-Pot, Metal-Free Conversion of Anilines to Aryl Bromides and Iodides. Organic Letters. 19(10). 2518–2521. 35 indexed citations
4.
Stack, Douglas E., John A. Conrad, & Bejan Mahmud. (2017). Structural Identification and Kinetic Analysis of thein VitroProducts Formed by Reaction of Bisphenol A-3,4-quinone withN-Acetylcysteine and Glutathione. Chemical Research in Toxicology. 31(2). 81–87. 11 indexed citations
5.
Stack, Douglas E., et al.. (2016). NMR analysis of t‐butyl‐catalyzed deuterium exchange at unactivated arene localities. Journal of Labelled Compounds and Radiopharmaceuticals. 59(12). 500–505. 6 indexed citations
6.
Stack, Douglas E.. (2015). Identifying the Tautomeric Form of a Deoxyguanosine-Estrogen Quinone Intermediate. Metabolites. 5(3). 475–488. 5 indexed citations
7.
Stack, Douglas E., et al.. (2014). Regioselective deuterium labeling of estrone and catechol estrogen metabolites. Steroids. 92. 32–38. 6 indexed citations
8.
Stack, Douglas E., et al.. (2008). Mechanistic Insights into the Michael Addition of Deoxyguanosine to Catechol Estrogen-3,4-quinones. Chemical Research in Toxicology. 21(7). 1415–1425. 15 indexed citations
9.
Stack, Douglas E., et al.. (2002). Synthesis of a New Fluorescent Probe Specific for Catechols. Organic Letters. 4(25). 4487–4490. 26 indexed citations
10.
Jankowiak, Ryszard, et al.. (1998). Spectral Characterization of Fluorescently Labeled Catechol Estrogen 3,4-Quinone-Derived N7 Guanine Adducts and Their Identification in Rat Mammary Gland Tissue. Chemical Research in Toxicology. 11(11). 1339–1345. 18 indexed citations
11.
Devanesan, Prabu, Douglas E. Stack, Ragulan Ramanathan, et al.. (1998). Metabolic Activation and Formation of DNA Adducts of Hexestrol, a Synthetic Nonsteroidal Carcinogenic Estrogen. Chemical Research in Toxicology. 11(5). 412–419. 37 indexed citations
12.
Cao, Kai, Douglas E. Stack, Ragulan Ramanathan, et al.. (1998). Synthesis and Structure Elucidation of Estrogen Quinones Conjugated with Cysteine, N-Acetylcysteine, and Glutathione. Chemical Research in Toxicology. 11(8). 909–916. 65 indexed citations
13.
Stack, Douglas E., Ercole L. Cavalieri, & Eleanor G. Rogan. (1997). Catecholestrogens as Procaroncinogens: Depurinating Adducts and Tumor Initiation. Advances in pharmacology. 42. 833–836. 11 indexed citations
14.
Stack, Douglas E., Jaeman Byun, Michael L. Gross, Eleanor G. Rogan, & Ercole L. Cavalieri. (1996). Molecular Characteristics of Catechol Estrogen Quinones in Reactions with Deoxyribonucleosides. Chemical Research in Toxicology. 9(5). 851–859. 170 indexed citations
15.
Casale, George P., Eleanor G. Rogan, Douglas E. Stack, Prabu Devanesan, & Ercole L. Cavalieri. (1996). Production and Immunochemical Characterization of a High-Affinity Monoclonal Antibody Specific for 7-(Benzo[a]pyren-6-yl)guanine (Bp-6-N7GUA), a Depurinating DNA Adduct of Benzo[a]pyrene. Polycyclic aromatic compounds. 10(1-4). 195–201. 1 indexed citations
16.
Stack, Douglas E., et al.. (1995). Radical cations of benzo[α]pyrene and 6-substituted derivatives: reaction with nucleophiles and DNA. Xenobiotica. 25(7). 755–760. 12 indexed citations
17.
Cremonesi, Paolo, Douglas E. Stack, Eleanor G. Rogan, & Ercole L. Cavalieri. (1994). Radical Cations of Benzo[a]pyrene and 6-Substituted Derivatives: Synthesis and Reaction with Nucleophiles. The Journal of Organic Chemistry. 59(25). 7683–7687. 15 indexed citations
18.
Stack, Douglas E. & Reuben D. Rieke. (1992). Formation of a new bis-organocopper reagent from the reaction of 2,3-dichloropropene and highly active zero valent copper derived from a CuCN·2LiCl complex. Tetrahedron Letters. 33(44). 6575–6578. 6 indexed citations
19.
Stack, Douglas E., et al.. (1992). Direct formation of highly functionalized allylic organocopper reagents from allylic chlorides and acetates. Journal of the American Chemical Society. 114(13). 5110–5116. 21 indexed citations
20.
Stack, Douglas E., et al.. (1991). Direct formation of functionalized and allylic organocopper reagents derived from a cuprous cyanide lithium bromide complex. Journal of the American Chemical Society. 113(12). 4672–4673. 36 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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