Alex G. Fallis

4.0k total citations
125 papers, 3.2k citations indexed

About

Alex G. Fallis is a scholar working on Organic Chemistry, Oncology and Molecular Biology. According to data from OpenAlex, Alex G. Fallis has authored 125 papers receiving a total of 3.2k indexed citations (citations by other indexed papers that have themselves been cited), including 110 papers in Organic Chemistry, 31 papers in Oncology and 14 papers in Molecular Biology. Recurrent topics in Alex G. Fallis's work include Synthetic Organic Chemistry Methods (51 papers), Asymmetric Synthesis and Catalysis (36 papers) and Cancer Treatment and Pharmacology (31 papers). Alex G. Fallis is often cited by papers focused on Synthetic Organic Chemistry Methods (51 papers), Asymmetric Synthesis and Catalysis (36 papers) and Cancer Treatment and Pharmacology (31 papers). Alex G. Fallis collaborates with scholars based in Canada, United States and United Kingdom. Alex G. Fallis's co-authors include Pat Forgione, Shawn K. Collins, Glenn P. A. Yap, Claudio F. Sturino, Matthew A. Heuft, Virendra Kumar Yadav, Simon Woo, Peter D. Wilson, Bo Lei and Curtis Harwig and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Accounts of Chemical Research.

In The Last Decade

Alex G. Fallis

123 papers receiving 3.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alex G. Fallis Canada 29 2.8k 541 187 178 176 125 3.2k
Arthur G. Schultz United States 28 2.4k 0.9× 549 1.0× 126 0.7× 156 0.9× 156 0.9× 178 2.8k
Ulf Pindur Germany 22 2.1k 0.8× 499 0.9× 116 0.6× 92 0.5× 121 0.7× 147 2.4k
Jean Suffert France 31 2.5k 0.9× 372 0.7× 154 0.8× 265 1.5× 128 0.7× 94 2.9k
Rick Danheiser United States 46 4.7k 1.7× 689 1.3× 123 0.7× 185 1.0× 244 1.4× 112 5.3k
Masazumi Ikeda Japan 29 3.4k 1.2× 740 1.4× 174 0.9× 87 0.5× 193 1.1× 289 3.7k
Yasumitsu Tamura Japan 27 3.1k 1.1× 651 1.2× 193 1.0× 90 0.5× 261 1.5× 303 3.4k
Ekkehard Winterfeldt Germany 27 2.7k 1.0× 996 1.8× 214 1.1× 77 0.4× 271 1.5× 213 3.3k
Akira Yoshikoshi Japan 23 2.0k 0.7× 768 1.4× 132 0.7× 114 0.6× 290 1.6× 143 2.6k
Larry Weiler Canada 25 1.5k 0.5× 514 1.0× 163 0.9× 156 0.9× 213 1.2× 98 2.1k
R. H. Schlessinger United States 29 2.1k 0.7× 558 1.0× 181 1.0× 119 0.7× 250 1.4× 123 2.5k

Countries citing papers authored by Alex G. Fallis

Since Specialization
Citations

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

Fields of papers citing papers by Alex G. Fallis

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alex G. Fallis. 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 Alex G. Fallis. The network helps show where Alex G. Fallis may publish in the future.

Co-authorship network of co-authors of Alex G. Fallis

This figure shows the co-authorship network connecting the top 25 collaborators of Alex G. Fallis. A scholar is included among the top collaborators of Alex G. Fallis 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 Alex G. Fallis. Alex G. Fallis 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.
Leclère, Mathieu & Alex G. Fallis. (2007). Asymmetric Allenophanes: Synthesis of a Tris‐meta‐allenophane and Tetrakis‐meta‐allenophane by Sequential Cross‐Coupling. Angewandte Chemie International Edition. 47(3). 568–572. 25 indexed citations
2.
Enright, G.D., et al.. (2007). Vinigrol:  A Compact, Diene-Transmissive Diels−Alder Strategy to the Tricyclic Core. Organic Letters. 9(25). 5163–5166. 35 indexed citations
3.
Leclère, Mathieu & Alex G. Fallis. (2007). Asymmetric Allenophanes: Synthesis of a Tris‐meta‐allenophane and Tetrakis‐meta‐allenophane by Sequential Cross‐Coupling. Angewandte Chemie. 120(3). 578–582. 17 indexed citations
4.
Fallis, Alex G., et al.. (2005). Acetylenic Allenophanes: An Asymmetric Synthesis of a Bis(alleno)‐bis(butadiynyl)‐meta‐cyclophane. Angewandte Chemie International Edition. 44(26). 4039–4042. 45 indexed citations
5.
Smil, David, Fabio E. S. Souza, & Alex G. Fallis. (2005). A general carbometalation, three component coupling strategy for the synthesis of α,β-unsaturated γ-sultines including thio-rofecoxib, a selective COX-2 inhibitor. Bioorganic & Medicinal Chemistry Letters. 15(8). 2057–2060. 14 indexed citations
6.
Heuft, Matthew A. & Alex G. Fallis. (2002). Template-Directed Synthesis of Helical Phenanthroline Cyclophanes. Angewandte Chemie International Edition. 41(23). 4520–4523. 26 indexed citations
7.
Collins, Shawn K., Glenn P. A. Yap, & Alex G. Fallis. (2000). The Synthesis of a Novel Strained Diyneparacyclophane and Its Dimer by Metal-Mediated Coupling. Angewandte Chemie International Edition. 39(2). 385–388. 43 indexed citations
8.
Forgione, Pat, Peter D. Wilson, & Alex G. Fallis. (2000). Magnesium mediated carbometallation of propargyl alcohols: direct routes to furans and furanones. Tetrahedron Letters. 41(1). 17–20. 40 indexed citations
9.
Fallis, Alex G.. (1999). Harvesting Diels and Alder's Garden: Synthetic Investigations of Intramolecular [4 + 2] Cycloadditions. Accounts of Chemical Research. 32(6). 464–474. 88 indexed citations
10.
Fallis, Alex G., et al.. (1999). Indium mediated γ-pentadienylation of conjugated aldehydes: synthons for hydrindanes by an oxy-Cope-cycloaddition strategy. Tetrahedron Letters. 40(45). 7867–7870. 18 indexed citations
11.
12.
Wilson, Peter D., et al.. (1997). Functionalization and elaboration of ring A taxoid building blocks. Canadian Journal of Chemistry. 75(11). 1542–1551. 7 indexed citations
13.
Fallis, Alex G., et al.. (1996). Dihydrofurans from α-diazoketones due to facile ring opening – cyclization of donor–acceptor cyclopropane intermediates. Canadian Journal of Chemistry. 74(12). 2401–2412. 10 indexed citations
14.
Fallis, Alex G., et al.. (1996). Tandem Radical Reactions:  Carbon Monoxide Addition to Alkyl Radicals and Subsequent Acyl Radical Cyclization onto N,N-Diphenylhydrazones. The Journal of Organic Chemistry. 61(11). 3580–3581. 25 indexed citations
15.
Fallis, Alex G., et al.. (1993). Dihydrofurans from α-diazoketones: Facile rearrangement of donor-acceptor cyclopropanes. Tetrahedron Letters. 34(43). 6841–6844. 16 indexed citations
16.
Fallis, Alex G., et al.. (1990). 分子内Diels-Alder反応を経る(+)-ロンギホレンの直接全合成. Journal of the American Chemical Society. 112(11). 4609–4610. 9 indexed citations
17.
Yadav, Virendra Kumar & Alex G. Fallis. (1988). Cyclopentane synthesis and annulation: Intramolecular radical cyclization of acetals. Tetrahedron Letters. 29(8). 897–900. 53 indexed citations
18.
Fallis, Alex G., et al.. (1988). .pi.-Facial selectivity: heteroatom directed syn/anti stereoselection in Diels-Alder cycloadditions of plane-nonsymmetric cyclopentadienes. Journal of the American Chemical Society. 110(12). 4074–4076. 28 indexed citations
19.
Gallacher, Gerard, et al.. (1984). Studies of intramolecular Diels–Alder reactions: preparation of methyl spiro[2.4]hepta-4,6-dien-1-yl esters and their internal cycloaddition reactivity. Canadian Journal of Chemistry. 62(9). 1709–1716. 9 indexed citations
20.

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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