Peter A. Wade

1.2k total citations
52 papers, 848 citations indexed

About

Peter A. Wade is a scholar working on Organic Chemistry, Molecular Biology and Physical and Theoretical Chemistry. According to data from OpenAlex, Peter A. Wade has authored 52 papers receiving a total of 848 indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Organic Chemistry, 12 papers in Molecular Biology and 9 papers in Physical and Theoretical Chemistry. Recurrent topics in Peter A. Wade's work include Chemical Reaction Mechanisms (16 papers), Chemical Synthesis and Analysis (10 papers) and Asymmetric Synthesis and Catalysis (10 papers). Peter A. Wade is often cited by papers focused on Chemical Reaction Mechanisms (16 papers), Chemical Synthesis and Analysis (10 papers) and Asymmetric Synthesis and Catalysis (10 papers). Peter A. Wade collaborates with scholars based in United States and Italy. Peter A. Wade's co-authors include Nathan Kornblum, Patrick J. Carroll, Melendhran Pillay, Steven A. Hardinger, William P. Dailey, Harold W. Pinnick, Ronald G. Smith, Robert C. Kerber, James Murray and Shri Singh and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

Peter A. Wade

51 papers receiving 777 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter A. Wade United States 18 755 274 97 80 68 52 848
William A. Smit Russia 20 1.0k 1.3× 164 0.6× 114 1.2× 95 1.2× 101 1.5× 80 1.1k
B. J. Wakefield United Kingdom 16 779 1.0× 178 0.6× 94 1.0× 56 0.7× 104 1.5× 94 924
Alfons L. Baumstark United States 14 487 0.6× 207 0.8× 88 0.9× 87 1.1× 45 0.7× 61 678
G. ZINNER Germany 15 767 1.0× 275 1.0× 128 1.3× 81 1.0× 58 0.9× 153 891
Ḡunadi Adiwidjaja Germany 16 866 1.1× 168 0.6× 37 0.4× 57 0.7× 108 1.6× 115 984
J. SAKATA Japan 8 653 0.9× 162 0.6× 86 0.9× 43 0.5× 111 1.6× 10 709
Ilya M. Lyapkalo Czechia 18 612 0.8× 120 0.4× 77 0.8× 40 0.5× 89 1.3× 39 710
Albert Heesing Germany 11 384 0.5× 133 0.5× 75 0.8× 73 0.9× 65 1.0× 79 475
Minoru Sekiya Japan 16 772 1.0× 199 0.7× 104 1.1× 84 1.1× 115 1.7× 150 886
Willy Friedrichsen Germany 17 991 1.3× 136 0.5× 106 1.1× 65 0.8× 40 0.6× 120 1.1k

Countries citing papers authored by Peter A. Wade

Since Specialization
Citations

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

Fields of papers citing papers by Peter A. Wade

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter A. Wade. 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 Peter A. Wade. The network helps show where Peter A. Wade may publish in the future.

Co-authorship network of co-authors of Peter A. Wade

This figure shows the co-authorship network connecting the top 25 collaborators of Peter A. Wade. A scholar is included among the top collaborators of Peter A. Wade 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 Peter A. Wade. Peter A. Wade 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.
Wade, Peter A., et al.. (2019). Nitration reactions of conjugated compounds employing lithium nitrate and trifluoroacetic anhydride. Canadian Journal of Chemistry. 97(8). 591–596. 2 indexed citations
2.
Wade, Peter A., et al.. (2015). Synthesis and conjugate addition reactions of N -(β-nitroalkyl)amides. Tetrahedron Letters. 56(48). 6722–6725. 5 indexed citations
3.
Wade, Peter A., et al.. (2013). Sequential Diels–Alder/[3,3]-sigmatropic rearrangement reactions of β-nitrostyrene with 3-methyl-1,3-pentadiene. Beilstein Journal of Organic Chemistry. 9. 2137–2146. 13 indexed citations
4.
Wade, Peter A., et al.. (2009). Reactions of (1‐nitroethenyl)sulfonylbenzene, a nitroethene derivative geminally substituted by a second W‐group. Journal of Physical Organic Chemistry. 22(4). 337–342. 3 indexed citations
5.
Xu, Hanying, Peter A. Wade, & Karl Sohlberg. (2009). Formation and sigmatropic rearrangement of PhCOC(NO2)CH2 cycloadducts of 1,3-cyclohexadiene: a theoretical study. Tetrahedron. 66(4). 845–851. 4 indexed citations
6.
Wade, Peter A., et al.. (2009). Formation and [3,3]-sigmatropic rearrangement of O-allyl nitronic esters: a new route to γ,δ-unsaturated nitro compounds. Chemical Communications. 3531–3531. 8 indexed citations
7.
Wade, Peter A., et al.. (2002). Competing Diels–Alder reactions of activated nitroethylene derivatives and [3,3]-sigmatropic rearrangements of the cycloadducts. Chemical Communications. 1090–1091. 16 indexed citations
8.
Wade, Peter A., et al.. (2002). Generation and in situ Diels–Alder reactions of activated nitroethylene derivatives. Tetrahedron Letters. 43(14). 2585–2588. 21 indexed citations
9.
Wade, Peter A., et al.. (2000). Tandem Nitroaldol−Dehydration Reactions Employing the Dianion of Phenylsulfonylnitromethane1. The Journal of Organic Chemistry. 65(23). 7723–7730. 8 indexed citations
10.
Wade, Peter A., et al.. (1997). Synthesis ofl-Daunosamine Derivatives on the Basis of the Asymmetric Dihydroxylation of 3-((E)-1-Propenyl)-4,5-dihydroisoxazole. The Journal of Organic Chemistry. 62(11). 3671–3677. 6 indexed citations
11.
Wade, Peter A., et al.. (1995). Autoxidation of [2-(1,3-dithianyl)]lithium: a cautionary note. The Journal of Organic Chemistry. 60(13). 4258–4259. 4 indexed citations
12.
Wade, Peter A., et al.. (1995). 2-Amino-2-Deoxytetrose Derivatives. 2. Preparation fromd-Glyceraldehyde Acetonide: A Reinvestigation. Journal of Carbohydrate Chemistry. 14(9). 1329–1341. 5 indexed citations
13.
Davis, Franklin A., et al.. (1993). Hydroxylation of dihydroisoxazoles using N-sulfonyloxaziridines. The Journal of Organic Chemistry. 58(26). 7591–7593. 17 indexed citations
14.
Wade, Peter A., et al.. (1989). A new route to 4-oxygenated isoxazolines. Application to the synthesis of 2-deoxy-2-aminobutose derivatives. Tetrahedron Letters. 30(10). 1185–1188. 14 indexed citations
15.
Wade, Peter A., et al.. (1989). A dihydroisoxazole-based route to 2,3,6-trideoxy-3-aminohexose derivatives. Tetrahedron Letters. 30(44). 5969–5972. 7 indexed citations
16.
Wade, Peter A., Harry Morrison, & Nathan Kornblum. (1987). Substitution reactions which proceed via radical anion intermediates. Part 30. Effect of light on electron transfer substitution at a saturated carbon atom. The Journal of Organic Chemistry. 52(14). 3102–3107. 27 indexed citations
17.
Wade, Peter A., Shankar M. Singh, & Melendhran Pillay. (1984). Benzenesulfonylcarbonitrile oxide. 5. Face selectivity of cycloaddition to chiral terminal alkenes. Tetrahedron. 40(3). 601–611. 30 indexed citations
18.
Wade, Peter A., et al.. (1983). Benzenesulfonylcarbonitrile oxide. 4. Substitution reactions of 3-phenylsulfonylisoxazolines. The Journal of Organic Chemistry. 48(11). 1796–1800. 18 indexed citations
19.
Wade, Peter A., et al.. (1982). Alkene Reductions Employing Ethyl Acetate-Hydroxylahine, a Useful new Source of Diimide. Synthetic Communications. 12(4). 287–291. 16 indexed citations
20.
Kornblum, Nathan, et al.. (1976). Displacement of the nitro group of substituted nitrobenzenes-a synthetically useful process. The Journal of Organic Chemistry. 41(9). 1560–1564. 108 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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