Alexander E. A. Porter

582 total citations
30 papers, 311 citations indexed

About

Alexander E. A. Porter is a scholar working on Organic Chemistry, Molecular Biology and Physical and Theoretical Chemistry. According to data from OpenAlex, Alexander E. A. Porter has authored 30 papers receiving a total of 311 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Organic Chemistry, 7 papers in Molecular Biology and 2 papers in Physical and Theoretical Chemistry. Recurrent topics in Alexander E. A. Porter's work include Cyclopropane Reaction Mechanisms (7 papers), Organic Chemistry Cycloaddition Reactions (6 papers) and Chemical Synthesis and Analysis (4 papers). Alexander E. A. Porter is often cited by papers focused on Cyclopropane Reaction Mechanisms (7 papers), Organic Chemistry Cycloaddition Reactions (6 papers) and Chemical Synthesis and Analysis (4 papers). Alexander E. A. Porter collaborates with scholars based in United Kingdom, Serbia and France. Alexander E. A. Porter's co-authors include Roger J. Gillespie, Suren Husinec, Derek H. R. Barton, David T. Coxon, Peter Murray‐Rust, R. Sexton, John W. Mansfıeld, Timothy M. Bowles, Judith Murray‐Rust and William B. Motherwell and has published in prestigious journals such as Journal of the American Chemical Society, Tetrahedron and Phytochemistry.

In The Last Decade

Alexander E. A. Porter

30 papers receiving 297 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Alexander E. A. Porter United Kingdom 10 215 90 34 23 19 30 311
Rolf Kyburz Switzerland 9 228 1.1× 70 0.8× 55 1.6× 22 1.0× 15 0.8× 11 322
M. Vandewalle Belgium 12 308 1.4× 118 1.3× 39 1.1× 37 1.6× 15 0.8× 32 424
Gary D. Annis United States 11 262 1.2× 88 1.0× 44 1.3× 22 1.0× 16 0.8× 15 401
Alfred Grieder Switzerland 10 234 1.1× 174 1.9× 21 0.6× 15 0.7× 13 0.7× 15 355
Masanori Yamaura Japan 12 247 1.1× 139 1.5× 47 1.4× 47 2.0× 17 0.9× 27 382
L. H. Zalkow United States 10 210 1.0× 177 2.0× 49 1.4× 28 1.2× 24 1.3× 29 385
Mary D. Menachery United States 10 183 0.9× 98 1.1× 62 1.8× 48 2.1× 12 0.6× 27 336
RI Willing Australia 14 200 0.9× 115 1.3× 61 1.8× 42 1.8× 12 0.6× 23 385
G. I. FEUTRILL Australia 10 231 1.1× 89 1.0× 27 0.8× 48 2.1× 13 0.7× 29 330
Nobushige Itaya Japan 12 167 0.8× 95 1.1× 110 3.2× 16 0.7× 30 1.6× 29 373

Countries citing papers authored by Alexander E. A. Porter

Since Specialization
Citations

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

Fields of papers citing papers by Alexander E. A. Porter

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Alexander E. A. Porter. 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 Alexander E. A. Porter. The network helps show where Alexander E. A. Porter may publish in the future.

Co-authorship network of co-authors of Alexander E. A. Porter

This figure shows the co-authorship network connecting the top 25 collaborators of Alexander E. A. Porter. A scholar is included among the top collaborators of Alexander E. A. Porter 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 Alexander E. A. Porter. Alexander E. A. Porter 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.
Bell, Michael V., James R. Dick, & Alexander E. A. Porter. (2003). Tissue deposition of n−3 FA pathway intermediates in the synthesis of DHA in rainbow trout (Oncorhynchus mykiss). Lipids. 38(9). 925–931. 9 indexed citations
2.
Juranić, Ivan O., Suren Husinec, Vladimir Savić, & Alexander E. A. Porter. (1991). Application of the MNDO method in planning the synthesis of Δ2-1,2,3-triazoles. Collection of Czechoslovak Chemical Communications. 56(2). 411–417. 5 indexed citations
3.
Bowles, Timothy M., et al.. (1988). Thermally induced rearrangement of thiopheniobis(alkoxycarbonyl)methanides. Journal of the Chemical Society Perkin Transactions 1. 803–803. 8 indexed citations
4.
Husinec, Suren, Vladimir Savić, & Alexander E. A. Porter. (1988). Azomethine ylids from diethyl aminomalonate. Tetrahedron Letters. 29(50). 6649–6650. 8 indexed citations
5.
Barton, Derek H. R., Timothy M. Bowles, Suren Husinec, et al.. (1988). Reductive formylation of oximes; an approach to the synthesis of vinyl isonitriles. Tetrahedron Letters. 29(27). 3343–3346. 31 indexed citations
6.
Porter, Alexander E. A. & Henry S. Rzepa. (1988). Thermally induced rearrangement of thiopheniobis(alkoxycarbonyl)methanides. A theoretical MNDO SCF-MO study. Journal of the Chemical Society Perkin Transactions 1. 809–809. 1 indexed citations
7.
Husinec, Suren, et al.. (1987). Approaches to the synthesis of kainic acid. A study of the synthesis of some 4,5-dihydro-1,2,3-triazoles. Collection of Czechoslovak Chemical Communications. 52(1). 207–214. 2 indexed citations
8.
9.
Bowles, Timothy M., et al.. (1984). A 1H n.m.r. and ab initio SCF-MO study of thiophenium methylides. Journal of the Chemical Society Chemical Communications. 859–859. 2 indexed citations
10.
11.
Husinec, Suren, et al.. (1984). Some approaches to the synthesis of kainic acid. Journal of the Chemical Society Perkin Transactions 1. 2517–2517. 21 indexed citations
12.
Porter, Alexander E. A., et al.. (1981). Synthesis of 2,5-dihydroxy-3,6-bis-(2-hydroxybenzyl)pyrazine. Journal of the Chemical Society Perkin Transactions 1. 3111–3111. 2 indexed citations
13.
Gillespie, Roger J., Judith Murray‐Rust, Peter Murray‐Rust, & Alexander E. A. Porter. (1981). A novel thermal rearrangement of the 2-thiabicyclo[3,1,0]hex-3-ene system. The crystal and molecular structure of ethyl-2,4-dichloro-5-hydroxy-6-methylbenzoate. Tetrahedron. 37(4). 743–746. 3 indexed citations
14.
Porter, Alexander E. A., et al.. (1980). Facile entry into the 7-oxo-4-oxo-1-azabicyclo[3.2.0]hept-2-ene ring system. Journal of the Chemical Society Chemical Communications. 1257–1257. 1 indexed citations
15.
Gillespie, Roger J. & Alexander E. A. Porter. (1979). Reaction of activated arenes with 2,5-dichlorothiophenium bismethoxycarbonylmethylide. Journal of the Chemical Society Chemical Communications. 50–50. 4 indexed citations
16.
Gillespie, Roger J. & Alexander E. A. Porter. (1979). The reaction of diazoalkanes with thiophen. Journal of the Chemical Society Perkin Transactions 1. 2624–2624. 19 indexed citations
17.
Gillespie, Roger J., et al.. (1978). 2,5-Dichlorothiophenium bismethoxycarbonylmethylide: a bismethoxycarbonylcarbene equivalent. Journal of the Chemical Society Chemical Communications. 641–641. 6 indexed citations
18.
Gillespie, Roger J., et al.. (1978). Thermal rearrangement of thiophenium bismethoxycarbonylmethylides: a novel synthesis of thiophene-2-malonic esters. Journal of the Chemical Society Chemical Communications. 85–85. 11 indexed citations
19.
Cox, Brian G., et al.. (1977). Long-range couplings in 2-alkoxycarbonylphenyl nitroxide radicals. Journal of the Chemical Society Perkin Transactions 2. 904–904. 1 indexed citations
20.
Cox, Brian G. & Alexander E. A. Porter. (1976). The general acid catalyzed displacement of amines from o-hydroxylaminobenzamides in aqueous and nonaqueous solvents. Journal of the American Chemical Society. 98(1). 159–162. 1 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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