John V. Turner

523 total citations
20 papers, 392 citations indexed

About

John V. Turner is a scholar working on Organic Chemistry, Molecular Biology and Cell Biology. According to data from OpenAlex, John V. Turner has authored 20 papers receiving a total of 392 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Organic Chemistry, 8 papers in Molecular Biology and 3 papers in Cell Biology. Recurrent topics in John V. Turner's work include Synthetic Organic Chemistry Methods (5 papers), Chemical Synthesis and Reactions (4 papers) and Chemical Synthesis and Analysis (3 papers). John V. Turner is often cited by papers focused on Synthetic Organic Chemistry Methods (5 papers), Chemical Synthesis and Reactions (4 papers) and Chemical Synthesis and Analysis (3 papers). John V. Turner collaborates with scholars based in Australia and United States. John V. Turner's co-authors include Lewis N. Mander, Robert D. Dawe, Tadeusz F. Molinski, Luciano Lombardo, John Orban, Srinivasan Chandrasekaran, Bruce Twitchin, С. Чандрасекаран, Russell A. Bell and Fernando Ferreira and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron Letters.

In The Last Decade

John V. Turner

20 papers receiving 355 citations

Peers

John V. Turner

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MB

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BIOTE

Luciano Lombardo Australia

Takuichi Miki Japan

Hiroko Akao Japan

Jeffrey M. Dener United States

D. Guillerm France

Daniela Borghi Italy

David J. Jebaratnam United States

G. HOEFLE Germany

H. G. DAVIES United Kingdom

H. TAKENO Japan

Luciano Lombardo Australia

John V. Turner

280 ×1.2

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119 ×0.7

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30 ×0.9

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31 ×1.0

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36 ×1.2

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Citations per year, relative to John V. Turner John V. Turner (= 1×) peers Luciano Lombardo

Countries citing papers authored by John V. Turner

Since Specialization

Citations

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

Fields of papers citing papers by John V. Turner

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John V. Turner. 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 John V. Turner. The network helps show where John V. Turner may publish in the future.

Co-authorship network of co-authors of John V. Turner

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

All Works

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20 of 20 papers shown

1.

Nguyen, Yen, et al.. (2019). Deprotection Strategies for Thioimidates during Fmoc Solid-Phase Peptide Synthesis: A Safe Route to Thioamides. The Journal of Organic Chemistry. 84(23). 15309–15314. 11 indexed citations

2.

Dellinger, Douglas J., Joel Myerson, Agnieszka Sierzchała, et al.. (2011). Streamlined Process for the Chemical Synthesis of RNA Using 2′-O-Thionocarbamate-Protected Nucleoside Phosphoramidites in the Solid Phase. Journal of the American Chemical Society. 133(30). 11540–11556. 53 indexed citations

3.

Dawe, Robert D., Lewis N. Mander, & John V. Turner. (1985). Stereocontrolled synthesis of gibberellin A19 from gibberellic acid. Tetrahedron Letters. 26(3). 363–366. 18 indexed citations

4.

Dawe, Robert D., Lewis N. Mander, John V. Turner, & Xinfu Pan. (1985). Syntheses of c20 gibberellin a36 and a37 methyl esters from gibberellic acid. Tetrahedron Letters. 26(46). 5725–5728. 15 indexed citations

5.

Orban, John, John V. Turner, & Bruce Twitchin. (1984). Preparation of -butyldimethylsilyl (tbdms) enol ethers using potassium hydride in the presence of tbdms chloride. Tetrahedron Letters. 25(44). 5099–5102. 10 indexed citations

6.

Dawe, Robert D., Tadeusz F. Molinski, & John V. Turner. (1984). Dilithium tetrabromonickelate (II) as a source of soft nucleophilic bromide : Reaction with epoxides. Tetrahedron Letters. 25(19). 2061–2064. 58 indexed citations

7.

Orban, John & John V. Turner. (1983). An economical diels-alder strategy for the synthesis of daphniphyllum alkaloids. Tetrahedron Letters. 24(26). 2697–2700. 17 indexed citations

8.

Чандрасекаран, С. & John V. Turner. (1982). Hybrid Birch-Claisen Methodology for arylation at allylic termini: synthesis of (±)-herbertene. Tetrahedron Letters. 23(37). 3799–3802. 10 indexed citations

9.

Chandrasekaran, Srinivasan & John V. Turner. (1982). A Mild and Versatile Method for Carboxy Group Activation and Esterification. Synthetic Communications. 12(9). 727–731. 23 indexed citations

10.

Mander, Lewis N. & John V. Turner. (1981). A highly convergent and flexible strategy for the synthesis of a-ring aromatic steroids. Tetrahedron Letters. 22(37). 3683–3686. 12 indexed citations

11.

Mander, Lewis N., John V. Turner, & Bruce Twitchin. (1981). Methodology for translocating the carboxy group in gibberellins: the partial synthesis of 7(6→15βH)-GA4. Tetrahedron Letters. 22(31). 3017–3020. 8 indexed citations

12.

Bell, Russell A. & John V. Turner. (1981). Stereoselective reduction of 3-keto gibberellin acids to 3β-ols using k-selectride with KH2PO4 buffer. Tetrahedron Letters. 22(48). 4871–4872. 9 indexed citations

13.

Mander, Lewis N. & John V. Turner. (1981). Chloroethoxy(trimethyl)silane: A hard-base trap which preserves tms ether groups and improves the wittig methylenation of gibberellins. Tetrahedron Letters. 22(41). 4149–4152. 14 indexed citations

14.

Lombardo, Luciano, Lewis N. Mander, & John V. Turner. (1980). General strategy for gibberellin synthesis: total syntheses of (.+-.)-gibberellin A1 and gibberellic acid. Journal of the American Chemical Society. 102(21). 6626–6628. 45 indexed citations

15.

Turner, John V., et al.. (1978). Tinidazole (TNZ) (ethyl[2-(2-methyl-5-nitro-1-imidazolyl) ethyl]sulphone) is mutagenic in a Salmonella typhimurium assay. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 57(2). 97–101. 4 indexed citations

16.

Turner, John V., A. David Ward, & Craig Freeman. (1978). The mutagenic screening of fourteen imidazo compounds using a modified ames' test. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 57(2). 135–139. 6 indexed citations

17.

Turner, John V., et al.. (1978). Tinidazole (TNZ) (ethyl[2-(2-methyl-5-nitro-1-imidazolyl) ethyl]sulphone) is mutagenic in a Salmonella typhimurium assay. Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 57(1). 97–101. 15 indexed citations

18.

Barrett, Anthony G. M., et al.. (1977). Transformations of penicillin. Part 8. Preparation of 2-acetylceph-3-em derivatives from carboxy-protected penicillin S-oxides. Journal of the Chemical Society Perkin Transactions 1. 1477–1477. 21 indexed citations

19.

Mander, Lewis N. & John V. Turner. (1973). Synthesis of .beta.,.gamma.-unsaturated aldehydes by the [2,3]-sigmatropic rearrangement of allylic ammonium ylides. The Journal of Organic Chemistry. 38(16). 2915–2916. 39 indexed citations

20.

Mander, LN & John V. Turner. (1973). ChemInform Abstract: THE SYNTHESIS OF BETA,GAMMA‐UNSATURATED ALDEHYDES BY (2,3)‐SIGMATROPIC REARRANGEMENT OF ALLYLIC AMMONIUM YLIDES. Chemischer Informationsdienst. 4(46). 4 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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