P. F. SCHUDA

1.2k total citations
27 papers, 815 citations indexed

About

P. F. SCHUDA is a scholar working on Organic Chemistry, Pharmacology and Molecular Biology. According to data from OpenAlex, P. F. SCHUDA has authored 27 papers receiving a total of 815 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 6 papers in Pharmacology and 4 papers in Molecular Biology. Recurrent topics in P. F. SCHUDA's work include Asymmetric Synthesis and Catalysis (9 papers), Advanced Synthetic Organic Chemistry (5 papers) and Chemical Synthesis and Reactions (4 papers). P. F. SCHUDA is often cited by papers focused on Asymmetric Synthesis and Catalysis (9 papers), Advanced Synthetic Organic Chemistry (5 papers) and Chemical Synthesis and Reactions (4 papers). P. F. SCHUDA collaborates with scholars based in United States. P. F. SCHUDA's co-authors include Samuel J. Danishefsky, Takeshi Kitahara, S. J. ETHEREDGE, William A. Price, R. L. McKee, Jennifer Phillips, Masahiro Hirama, William J. Greenlee, Probir Chakravarty and Philip Eskola and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

P. F. SCHUDA

27 papers receiving 762 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
P. F. SCHUDA United States 16 641 244 99 93 59 27 815
Drury Caine United States 17 620 1.0× 159 0.7× 79 0.8× 83 0.9× 53 0.9× 71 747
S. GILMAN 6 591 0.9× 190 0.8× 116 1.2× 90 1.0× 38 0.6× 6 716
Michiharu Kato Japan 16 608 0.9× 212 0.9× 67 0.7× 86 0.9× 46 0.8× 71 799
Anwer Basha Pakistan 15 775 1.2× 418 1.7× 76 0.8× 110 1.2× 27 0.5× 38 1.0k
J. E. Saxton United Kingdom 16 836 1.3× 254 1.0× 54 0.5× 121 1.3× 33 0.6× 49 1.0k
James Kallmerten United States 18 535 0.8× 147 0.6× 63 0.6× 103 1.1× 32 0.5× 43 673
O. Achmatowicz Poland 17 825 1.3× 347 1.4× 95 1.0× 161 1.7× 27 0.5× 60 1.1k
Yoshinobu Inouye Japan 16 493 0.8× 267 1.1× 155 1.6× 142 1.5× 40 0.7× 62 837
Morio Asaoka Japan 16 685 1.1× 194 0.8× 107 1.1× 56 0.6× 27 0.5× 66 792
Kunio Ogasawara Japan 18 885 1.4× 268 1.1× 88 0.9× 96 1.0× 28 0.5× 60 1.0k

Countries citing papers authored by P. F. SCHUDA

Since Specialization
Citations

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

Fields of papers citing papers by P. F. SCHUDA

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P. F. SCHUDA. 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 P. F. SCHUDA. The network helps show where P. F. SCHUDA may publish in the future.

Co-authorship network of co-authors of P. F. SCHUDA

This figure shows the co-authorship network connecting the top 25 collaborators of P. F. SCHUDA. A scholar is included among the top collaborators of P. F. SCHUDA 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 P. F. SCHUDA. P. F. SCHUDA 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.
Chakravarty, Prasun K., et al.. (1989). The synthesis of (2S,4S,5S) -5-(N-BOC)-amino-6-cyclohexyl-4-hydroxy-2-isopropyl-hexanoic acid lactone, an hydroxyethylene dipeptide isostere precusor. Tetrahedron Letters. 30(4). 415–418. 33 indexed citations
2.
SCHUDA, P. F. & William A. Price. (1987). Total synthesis of isoflavones: jamaicin, calopogonium isoflavone-B, pseudobaptigenin, and maxima substance-B. Friedel-Crafts acylation reactions with acid-sensitive substrates. The Journal of Organic Chemistry. 52(10). 1972–1979. 67 indexed citations
3.
4.
SCHUDA, P. F., et al.. (1987). The Synthesis of 4-Oxo-2-pentenoic Esters by Wittig Reaction Using α-Oxoesters. Synthesis. 1987(12). 1055–1057. 24 indexed citations
5.
SCHUDA, P. F. & Jennifer Phillips. (1984). A short synthesis of 2H‐1‐benzopyrans. Journal of Heterocyclic Chemistry. 21(3). 669–672. 3 indexed citations
6.
SCHUDA, P. F., et al.. (1984). A SYNTHESIS OF THE SIDEROPHORE 1,3,5-TRIS(N,N′,N-2,3-DIHYDROXYBENZOYL)AMINOMETHYLBENZENE. Organic Preparations and Procedures International. 16(2). 119–125. 3 indexed citations
7.
SCHUDA, P. F., et al.. (1984). The synthesis of dl-coriolin. Tetrahedron. 40(12). 2365–2380. 17 indexed citations
8.
SCHUDA, P. F., et al.. (1983). The synthesis of dl-Coriolin. Tetrahedron Letters. 24(40). 4267–4270. 13 indexed citations
9.
SCHUDA, P. F., et al.. (1983). A facile method for the oxidative removal of benzyl ethers: the oxidation of benzyl ethers to benzoates by ruthenium tetraoxide. Tetrahedron Letters. 24(36). 3829–3830. 58 indexed citations
10.
SCHUDA, P. F., et al.. (1982). Synthesis of coriolin. An approach to a functionalized BC ring system. The Journal of Organic Chemistry. 47(18). 3434–3440. 12 indexed citations
11.
Buechi, George, et al.. (1981). New synthesis of aflatoxin M1. Journal of the American Chemical Society. 103(12). 3497–3501. 19 indexed citations
12.
Hirama, Masahiro, et al.. (1980). ChemInform Abstract: TOTAL SYNTHESIS OF DL‐PENTALENOLACTONE. Chemischer Informationsdienst. 11(7). 2 indexed citations
13.
Danishefsky, Samuel J., et al.. (1979). Total synthesis of dl-pentalenolactone. Journal of the American Chemical Society. 101(23). 7020–7031. 38 indexed citations
14.
Danishefsky, Samuel J., et al.. (1978). Stereospecific total synthesis of dl-pentalenolactone. Journal of the American Chemical Society. 100(20). 6536–6538. 38 indexed citations
15.
Danishefsky, Samuel J., et al.. (1977). A dramatic solvent effect in the Diels-Alder reactions of o-benzoquinones. The Journal of Organic Chemistry. 42(12). 2179–2180. 12 indexed citations
16.
Danishefsky, Samuel J., P. F. SCHUDA, Takeshi Kitahara, & S. J. ETHEREDGE. (1977). The total synthesis of dl-vernolepin and dl-vernomenin. Journal of the American Chemical Society. 99(18). 6066–6075. 106 indexed citations
17.
Danishefsky, Samuel J., P. F. SCHUDA, Samuel M. Mazza, & Kuniki Kato. (1976). Diels-Alder reactions of o-benzoquinones. A route to derivatives of .DELTA.2-1-octalone. The Journal of Organic Chemistry. 41(21). 3468–3473. 15 indexed citations
18.
Danishefsky, Samuel J., Takeshi Kitahara, P. F. SCHUDA, & S. J. ETHEREDGE. (1976). A remarkable epoxide opening. An expeditious synthesis of vernolepin and vernomenin. Journal of the American Chemical Society. 98(10). 3028–3030. 39 indexed citations
19.
Danishefsky, Samuel J., Takeshi Kitahara, R. L. McKee, & P. F. SCHUDA. (1976). Reactions of silyl enol ethers and lactone enolates with dimethyl(methylene)ammonium iodide. The bis-.alpha.-methylenation of pre-vernolepin and pre-vernomenin. Journal of the American Chemical Society. 98(21). 6715–6717. 120 indexed citations
20.
Danishefsky, Samuel J., et al.. (1976). Synthesis of vernolepin. Diels-Alder approach to the angularly functionalized AB system. The Journal of Organic Chemistry. 41(7). 1081–1088. 15 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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