William J. DuBay

553 total citations
18 papers, 422 citations indexed

About

William J. DuBay is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, William J. DuBay has authored 18 papers receiving a total of 422 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Organic Chemistry, 2 papers in Inorganic Chemistry and 1 paper in Molecular Biology. Recurrent topics in William J. DuBay's work include Synthetic Organic Chemistry Methods (7 papers), Catalytic Alkyne Reactions (4 papers) and Asymmetric Synthesis and Catalysis (4 papers). William J. DuBay is often cited by papers focused on Synthetic Organic Chemistry Methods (7 papers), Catalytic Alkyne Reactions (4 papers) and Asymmetric Synthesis and Catalysis (4 papers). William J. DuBay collaborates with scholars based in United States. William J. DuBay's co-authors include James A. Marshall, T. Howard Black, Paul A. Grieco, Lee J. Todd, Charles L. Liotta, Paméla Pollet, Kenneth J. Henry, Charles A. Eckert, Jeffrey D. Butler and Grant M. Kloster and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Industrial & Engineering Chemistry Research.

In The Last Decade

William J. DuBay

17 papers receiving 400 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
William J. DuBay United States 15 353 58 43 41 27 18 422
Michael C. Weismiller United States 9 319 0.9× 59 1.0× 65 1.5× 30 0.7× 12 0.4× 12 418
Roman Davis United States 10 281 0.8× 64 1.1× 114 2.7× 38 0.9× 12 0.4× 23 376
Dalian Zhao United States 14 331 0.9× 81 1.4× 152 3.5× 44 1.1× 10 0.4× 20 448
Jaimala R. Ahuja India 9 339 1.0× 76 1.3× 97 2.3× 14 0.3× 14 0.5× 11 400
Julio C. Podestá Argentina 14 517 1.5× 112 1.9× 72 1.7× 27 0.7× 10 0.4× 57 570
Shinjiro Sumi Japan 6 258 0.7× 24 0.4× 43 1.0× 47 1.1× 19 0.7× 6 340
Chi Sun Hahn South Korea 9 259 0.7× 39 0.7× 82 1.9× 16 0.4× 15 0.6× 17 312
Richard G. Wilde United States 12 487 1.4× 58 1.0× 85 2.0× 15 0.4× 22 0.8× 19 597
Boyapati Veeranjaneyulu India 9 359 1.0× 69 1.2× 53 1.2× 11 0.3× 16 0.6× 20 386
Harish Holla India 14 526 1.5× 107 1.8× 116 2.7× 28 0.7× 17 0.6× 42 616

Countries citing papers authored by William J. DuBay

Since Specialization
Citations

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

Fields of papers citing papers by William J. DuBay

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by William J. DuBay. 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 William J. DuBay. The network helps show where William J. DuBay may publish in the future.

Co-authorship network of co-authors of William J. DuBay

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

All Works

18 of 18 papers shown
1.
Gelbaum, Leslie T., Paméla Pollet, William J. DuBay, et al.. (2013). Indoles via Knoevenagel–Hemetsberger reaction sequence. RSC Advances. 3(32). 13232–13232. 26 indexed citations
2.
Pollet, Paméla, et al.. (2012). Al(OtBu)3 as an Effective Catalyst for the Enhancement of Meerwein–Ponndorf–Verley (MPV) Reductions. Organic Process Research & Development. 16(7). 1301–1306. 15 indexed citations
3.
Pollet, Paméla, et al.. (2009). Production of (S)-1-Benzyl-3-diazo-2-oxopropylcarbamic Acid tert-Butyl Ester, a Diazoketone Pharmaceutical Intermediate, Employing a Small Scale Continuous Reactor. Industrial & Engineering Chemistry Research. 48(15). 7032–7036. 24 indexed citations
4.
Kloster, Grant M., et al.. (1997). Nb(OCH(CF3)2)6−: prototype for a new class of weakly coordinating anions based on polyfluoroalkoxide substituents. Inorganica Chimica Acta. 263(1-2). 195–200. 19 indexed citations
5.
Henry, Kenneth J., Paul A. Grieco, & William J. DuBay. (1996). A novel approach to iboga alkaloids: Total synthesis of (±)-ibogamine and (±)-epi-ibogamine. Tetrahedron Letters. 37(46). 8289–8292. 19 indexed citations
6.
Grieco, Paul A., William J. DuBay, & Lee J. Todd. (1996). Lithium cobalt-bis-dicarbollide catalyzed substitution reactions of allylic acetates. Tetrahedron Letters. 37(48). 8707–8710. 18 indexed citations
7.
Marshall, James A. & William J. DuBay. (1994). Synthesis of the Pseudopterane and Furanocembrane Ring Systems by Intraannular Cyclization of .beta.- and .gamma.-Alkynyl Allylic Alcohols. The Journal of Organic Chemistry. 59(7). 1703–1708. 49 indexed citations
8.
9.
10.
DuBay, William J., Paul A. Grieco, & Lee J. Todd. (1994). Lithium Cobalt-Bis-Dicarbollide: A Novel Lewis Acid Catalyst for the Conjugate Addition of Silyl Ketene Acetals to Hindered .alpha.,.beta.-Unsaturated Carbonyl Compounds. The Journal of Organic Chemistry. 59(23). 6898–6899. 20 indexed citations
11.
Marshall, James A. & William J. DuBay. (1993). Synthesis of furans by base-catalyzed cyclization-isomerization of .beta.- and .gamma.-alkynyl allylic alcohols. The Journal of Organic Chemistry. 58(12). 3435–3443. 50 indexed citations
12.
Marshall, James A. & William J. DuBay. (1993). A New Synthesis of Thiophenes Through Base-Promoted Cyclization of β- and γ-Alkynyl Thiols. Synlett. 1993(3). 209–210. 7 indexed citations
13.
Marshall, James A. & William J. DuBay. (1993). Synthesis of rosefuran. A new route to furans through base-catalyzed cyclization of hydroxy alkynoates and alkynones. The Journal of Organic Chemistry. 58(14). 3602–3603. 33 indexed citations
14.
Marshall, James A. & William J. DuBay. (1992). Base-catalyzed isomerization of alkynyloxiranes. A general synthesis of furans. Journal of the American Chemical Society. 114(4). 1450–1456. 41 indexed citations
15.
Marshall, James A. & William J. DuBay. (1991). A novel synthesis of furans by base-catalyzed isomerization of alkynyloxiranes. The Journal of Organic Chemistry. 56(5). 1685–1687. 20 indexed citations
16.
Black, T. Howard, et al.. (1988). Dyotropic rearrangement of cycloalkyl .beta.-lactones. Formation of spiro versus fused butyrolactones as a function of ring size. The Journal of Organic Chemistry. 53(25). 5922–5927. 35 indexed citations
17.
Black, T. Howard & William J. DuBay. (1988). Lactone synthesis via dyotropic rearrangement. Stereospecific construction of fused butyrolactones with three contiguous asymmetric centers. Tetrahedron Letters. 29(15). 1747–1750. 24 indexed citations
18.
Black, T. Howard & William J. DuBay. (1987). A new synthesis of substituted spiro butyrolactones via dyotropic rearrangement. Tetrahedron Letters. 28(41). 4787–4788. 20 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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