Eda Canales

1.5k total citations
16 papers, 776 citations indexed

About

Eda Canales is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Eda Canales has authored 16 papers receiving a total of 776 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Organic Chemistry, 5 papers in Inorganic Chemistry and 2 papers in Molecular Biology. Recurrent topics in Eda Canales's work include Asymmetric Synthesis and Catalysis (12 papers), Synthetic Organic Chemistry Methods (8 papers) and Asymmetric Hydrogenation and Catalysis (5 papers). Eda Canales is often cited by papers focused on Asymmetric Synthesis and Catalysis (12 papers), Synthetic Organic Chemistry Methods (8 papers) and Asymmetric Hydrogenation and Catalysis (5 papers). Eda Canales collaborates with scholars based in Puerto Rico and United States. Eda Canales's co-authors include John A. Soderquist, E. J. Corey, Ana Z. González, Karl Matos, Carlos H. Burgos, Duan Liu, Eliud Hernandez O'Farril, Eduvigis González, Brad R. Weiner and Gerardo Morell and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Antimicrobial Agents and Chemotherapy.

In The Last Decade

Eda Canales

16 papers receiving 772 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Eda Canales Puerto Rico 13 711 151 149 29 24 16 776
Shiping Xie United States 13 379 0.5× 88 0.6× 200 1.3× 17 0.6× 19 0.8× 22 510
Darryl G. Cleary United States 10 409 0.6× 78 0.5× 138 0.9× 31 1.1× 78 3.3× 16 507
Jonas Brånalt Sweden 12 426 0.6× 98 0.6× 180 1.2× 26 0.9× 19 0.8× 19 572
Stéphane Perreault United States 11 681 1.0× 79 0.5× 148 1.0× 10 0.3× 21 0.9× 12 762
Mousumi Sannigrahi Canada 11 517 0.7× 49 0.3× 89 0.6× 15 0.5× 12 0.5× 21 581
Kevin M. Belyk United States 20 824 1.2× 291 1.9× 309 2.1× 14 0.5× 55 2.3× 31 1.0k
Alan Millar United States 10 379 0.5× 53 0.4× 159 1.1× 21 0.7× 15 0.6× 16 511
Deborah C. Reuter United States 11 402 0.6× 51 0.3× 196 1.3× 15 0.5× 22 0.9× 12 576
S. P. MCKEE United States 14 483 0.7× 52 0.3× 293 2.0× 11 0.4× 14 0.6× 20 702
Bhavanam Sekhara Reddy India 9 838 1.2× 145 1.0× 256 1.7× 15 0.5× 16 0.7× 13 933

Countries citing papers authored by Eda Canales

Since Specialization
Citations

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

Fields of papers citing papers by Eda Canales

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Eda Canales. 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 Eda Canales. The network helps show where Eda Canales may publish in the future.

Co-authorship network of co-authors of Eda Canales

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

All Works

16 of 16 papers shown
1.
Pokrovskii, Maria, Philip Morganelli, Eda Canales, et al.. (2013). A Small-Molecule Inhibitor of Hepatitis C Virus Infectivity. Antimicrobial Agents and Chemotherapy. 58(1). 386–396. 18 indexed citations
2.
Canales, Eda, Joseph S. Carlson, T.C. Appleby, et al.. (2012). Tri-substituted acylhydrazines as tertiary amide bioisosteres: HCV NS5B polymerase inhibitors. Bioorganic & Medicinal Chemistry Letters. 22(13). 4288–4292. 13 indexed citations
3.
Canales, Eda & E. J. Corey. (2009). Synthesis of Estrone Methyl Ether. Synfacts. 2009(2). 117–117. 1 indexed citations
4.
González, Ana Z., et al.. (2008). Borabicyclo[3.3.2]decanes and the Stereoselective Asymmetric Synthesis of 1,3-Diol Stereotriads from 1,3-Diborylpropenes. Journal of the American Chemical Society. 131(3). 1269–1273. 62 indexed citations
5.
Canales, Eda & E. J. Corey. (2008). Highly Enantioselective [4 + 2] Cycloaddition Reactions Catalyzed by a Chiral N-Methyl-oxazaborolidinium Cation. Organic Letters. 10(15). 3271–3273. 46 indexed citations
6.
Canales, Eda & E. J. Corey. (2007). Highly Enantioselective [2+2]-Cycloaddition Reactions Catalyzed by a Chiral Aluminum Bromide Complex. Journal of the American Chemical Society. 129(42). 12686–12687. 136 indexed citations
7.
Liu, Duan, Eda Canales, & E. J. Corey. (2007). Chiral Oxazaborolidine−Aluminum Bromide Complexes Are Unusually Powerful and Effective Catalysts for Enantioselective Diels−Alder Reactions. Journal of the American Chemical Society. 129(6). 1498–1499. 100 indexed citations
8.
Canales, Eda, Ana Z. González, & John A. Soderquist. (2006). Asymmetric Synthesis of Isomerically Pure Allenyl Boranes from Alkynyl Boranes through a 1,2‐Insertion–1,3‐Borotropic Rearrangement. Angewandte Chemie International Edition. 46(3). 397–399. 48 indexed citations
9.
Canales, Eda, et al.. (2006). Enantioselective Allylboration ofN-Trimethylsilylketimines. Synfacts. 2006(10). 1052–1052. 1 indexed citations
10.
Canales, Eda, Ana Z. González, & John A. Soderquist. (2006). Asymmetric Synthesis of Isomerically Pure Allenyl Boranes from Alkynyl Boranes through a 1,2‐Insertion–1,3‐Borotropic Rearrangement. Angewandte Chemie. 119(3). 401–403. 12 indexed citations
11.
Canales, Eda, Eliud Hernandez O'Farril, & John A. Soderquist. (2006). Nonracemic 3°-Carbamines from the Asymmetric Allylboration of N-Trimethylsilyl Ketimines with B-Allyl-10-phenyl-9-borabicyclo[3.3.2]decanes. Journal of the American Chemical Society. 128(27). 8712–8713. 39 indexed citations
12.
O'Farril, Eliud Hernandez, Eda Canales, Eduvigis González, & John A. Soderquist. (2006). Asymmetric synthesis with the robust and versatile 10-substituted 9-borabicyclo[3.3.2]decanes: Homoallylic amines from aldimines. Pure and Applied Chemistry. 78(7). 1389–1395. 28 indexed citations
13.
González, Ana Z., Eda Canales, & John A. Soderquist. (2006). N-Propargylamides via the Asymmetric Michael Addition of B-Alkynyl-10-TMS-9- borabicyclo[3.3.2]decanes to N-Acylimines. Organic Letters. 8(15). 3331–3334. 35 indexed citations
14.
Canales, Eda, et al.. (2005). B-Allyl-10-Ph-9-borabicyclo[3.3.2]decanes:  Strategically Designed for the Asymmetric Allylboration of Ketones. Journal of the American Chemical Society. 127(33). 11572–11573. 90 indexed citations
15.
Burgos, Carlos H., Eda Canales, Karl Matos, & John A. Soderquist. (2005). Asymmetric Allyl- and Crotylboration with the Robust, Versatile, and Recyclable 10-TMS-9-borabicyclo[3.3.2]decanes. Journal of the American Chemical Society. 127(22). 8044–8049. 133 indexed citations
16.
Morell, Gerardo, Eda Canales, & Brad R. Weiner. (1999). In situ measurements of methane and acetylene concentrations in a CVD reactor by infrared spectroscopy. Diamond and Related Materials. 8(2-5). 166–170. 14 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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