B.O. Ashburn

476 total citations
18 papers, 399 citations indexed

About

B.O. Ashburn is a scholar working on Organic Chemistry, Infectious Diseases and Public Health, Environmental and Occupational Health. According to data from OpenAlex, B.O. Ashburn has authored 18 papers receiving a total of 399 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Organic Chemistry, 2 papers in Infectious Diseases and 2 papers in Public Health, Environmental and Occupational Health. Recurrent topics in B.O. Ashburn's work include Asymmetric Synthesis and Catalysis (9 papers), Axial and Atropisomeric Chirality Synthesis (6 papers) and Synthesis and biological activity (5 papers). B.O. Ashburn is often cited by papers focused on Asymmetric Synthesis and Catalysis (9 papers), Axial and Atropisomeric Chirality Synthesis (6 papers) and Synthesis and biological activity (5 papers). B.O. Ashburn collaborates with scholars based in United States. B.O. Ashburn's co-authors include Rich G. Carter, Lev N. Zakharov, David A. Vicic, Marcus A. Tius, A. K. Basak, Naoyuki Shimada, Nicholas Bailey, Paul Ha‐Yeon Cheong and Ryne C. Johnston and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and SHILAP Revista de lepidopterología.

In The Last Decade

B.O. Ashburn

18 papers receiving 395 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
B.O. Ashburn United States 11 358 65 55 24 11 18 399
Brian S. Bodnar United States 5 372 1.0× 60 0.9× 42 0.8× 12 0.5× 15 1.4× 6 398
Boyapati Veeranjaneyulu India 9 359 1.0× 53 0.8× 69 1.3× 38 1.6× 13 1.2× 20 386
Guang Yu Fang United Kingdom 13 553 1.5× 66 1.0× 99 1.8× 18 0.8× 19 1.7× 17 586
Paul F. Vogt United States 7 337 0.9× 99 1.5× 64 1.2× 14 0.6× 21 1.9× 17 397
Steffen Mader Germany 10 499 1.4× 82 1.3× 128 2.3× 15 0.6× 7 0.6× 13 542
Jianxie Chen Japan 12 345 1.0× 88 1.4× 80 1.5× 15 0.6× 21 1.9× 18 384
Bhaskar Deka India 12 382 1.1× 42 0.6× 39 0.7× 28 1.2× 16 1.5× 16 416
Carolyn S. Wei United States 10 381 1.1× 46 0.7× 103 1.9× 22 0.9× 17 1.5× 14 414
Ulf Scheffler Germany 9 415 1.2× 136 2.1× 117 2.1× 22 0.9× 14 1.3× 11 479
Rika Takagi Japan 6 369 1.0× 87 1.3× 126 2.3× 13 0.5× 9 0.8× 6 399

Countries citing papers authored by B.O. Ashburn

Since Specialization
Citations

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

Fields of papers citing papers by B.O. Ashburn

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by B.O. Ashburn. 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 B.O. Ashburn. The network helps show where B.O. Ashburn may publish in the future.

Co-authorship network of co-authors of B.O. Ashburn

This figure shows the co-authorship network connecting the top 25 collaborators of B.O. Ashburn. A scholar is included among the top collaborators of B.O. Ashburn 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 B.O. Ashburn. B.O. Ashburn 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.
Ashburn, B.O., et al.. (2022). (E)-3-[4-(1H-Imidazol-1-yl)phenyl]-1-(3-chloro-4-fluorophenyl)prop-2-en-1-one. SHILAP Revista de lepidopterología. 2022(2). M1375–M1375. 1 indexed citations
2.
Bailey, Nicholas, et al.. (2021). (E)-3-(4-Chlorophenyl)-1-(2-fluoro-4-methoxyphenyl)-2-propen-1-one. SHILAP Revista de lepidopterología. 2021(1). M1184–M1184. 5 indexed citations
3.
Ashburn, B.O.. (2021). Synthesis of Heterocyclic Chalcones as Novel Antileishmanial Agents. The FASEB Journal. 35(S1). 1 indexed citations
4.
Bailey, Nicholas & B.O. Ashburn. (2021). (E)-3-[4-(1H-Imidazol-1-yl)phenyl]-1-(4-methylphenyl)prop-2-en-1-one. SHILAP Revista de lepidopterología. 2021(3). M1269–M1269. 2 indexed citations
5.
Ashburn, B.O., et al.. (2020). Lipophilicity Determination of Energy-Enhancing, Nootropic Supplements. 1 indexed citations
6.
Ashburn, B.O.. (2019). Computational Analysis of a Series of Chlorinated Chalcone Derivatives. 7(4). 106–120. 6 indexed citations
7.
Ashburn, B.O., et al.. (2018). Computational Analysis of Theacrine, a Purported Nootropic and Energy-Enhancing Nutritional Supplement. 7(1). 27–37. 12 indexed citations
8.
Ashburn, B.O., et al.. (2012). Highly regioselective nitrile oxide dipolar cycloadditions with ortho-nitrophenyl alkynes. Organic & Biomolecular Chemistry. 10(46). 9204–9204. 28 indexed citations
9.
Johnston, Ryne C., et al.. (2012). Synthesis and Computational Analysis of Densely Functionalized Triazoles Using o-Nitrophenylalkynes. The Journal of Organic Chemistry. 77(2). 1101–1112. 17 indexed citations
10.
Shimada, Naoyuki, et al.. (2010). Organocatalytic asymmetric aza-Nazarov cyclization of an azirine. Chemical Communications. 46(21). 3774–3774. 65 indexed citations
11.
Ashburn, B.O., Rich G. Carter, & Lev N. Zakharov. (2008). Diels−Alder Approach to Biaryls: Elucidation of Competing Tandem [2+2] Cycloaddition/[1,3] Sigmatropic Shift Pathway. The Journal of Organic Chemistry. 73(18). 7305–7309. 23 indexed citations
12.
Ashburn, B.O. & Rich G. Carter. (2008). Diels–Alder approach to biaryls (DAB): Importance of the ortho-nitro moiety in the [4 + 2] cycloaddition. Organic & Biomolecular Chemistry. 6(2). 255–257. 13 indexed citations
13.
Ashburn, B.O. & Rich G. Carter. (2007). Diels−Alder Approach to Tetra-ortho-Substituted Biaryls Employing Propargylic Tertiary Alcohols as Dienophiles. The Journal of Organic Chemistry. 72(26). 10220–10223. 14 indexed citations
14.
Ashburn, B.O., et al.. (2007). Diels−Alder Approach for the Construction of Halogenated, o-Nitro Biaryl Templates and Application to the Total Synthesis of the Anti-HIV Agent Siamenol. The Journal of Organic Chemistry. 72(26). 9857–9865. 51 indexed citations
15.
Ashburn, B.O., et al.. (2007). A Diels–Alder approach to biaryls (DAB): synthesis of the western portion of TMC-95. Tetrahedron. 64(5). 856–865. 18 indexed citations
16.
Ashburn, B.O., Rich G. Carter, & Lev N. Zakharov. (2007). Synthesis of Tetra-ortho-substituted, Phosphorus-Containing and Carbonyl-Containing Biaryls Utilizing a Diels−Alder Approach. Journal of the American Chemical Society. 129(29). 9109–9116. 71 indexed citations
17.
Ashburn, B.O. & Rich G. Carter. (2006). Diels–Alder Approach to Polysubstituted Biaryls: Rapid Entry to Tri‐ and Tetra‐ortho‐substituted Phosphorus‐Containing Biaryls. Angewandte Chemie International Edition. 45(40). 6737–6741. 61 indexed citations
18.
Ashburn, B.O. & Rich G. Carter. (2006). Diels–Alder Approach to Polysubstituted Biaryls: Rapid Entry to Tri‐ and Tetra‐ortho‐substituted Phosphorus‐Containing Biaryls. Angewandte Chemie. 118(40). 6889–6893. 10 indexed citations

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