David M. Hollinshead

650 total citations
17 papers, 450 citations indexed

About

David M. Hollinshead is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, David M. Hollinshead has authored 17 papers receiving a total of 450 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Organic Chemistry, 5 papers in Molecular Biology and 3 papers in Inorganic Chemistry. Recurrent topics in David M. Hollinshead's work include Synthesis and Catalytic Reactions (4 papers), Synthesis of β-Lactam Compounds (4 papers) and Oxidative Organic Chemistry Reactions (3 papers). David M. Hollinshead is often cited by papers focused on Synthesis and Catalytic Reactions (4 papers), Synthesis of β-Lactam Compounds (4 papers) and Oxidative Organic Chemistry Reactions (3 papers). David M. Hollinshead collaborates with scholars based in United Kingdom, Sweden and Netherlands. David M. Hollinshead's co-authors include Steven V. Ley, Simon T. Hodgson, Martin Schröder, William P. Griffith, Norman M. Ratcliffe, Paul A. Worthington, S. C. Howell, Julian G. Knight, Duncan Armour and Simon J. Harwood and has published in prestigious journals such as Journal of the American Chemical Society, Nature Communications and Journal of Medicinal Chemistry.

In The Last Decade

David M. Hollinshead

17 papers receiving 413 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
David M. Hollinshead United Kingdom 13 320 119 55 50 42 17 450
T. HATAJIMA Japan 6 548 1.7× 126 1.1× 85 1.5× 53 1.1× 42 1.0× 7 625
Vance J. Novack United States 7 407 1.3× 114 1.0× 53 1.0× 51 1.0× 65 1.5× 11 469
Kimikazu Nakamura Japan 3 578 1.8× 150 1.3× 82 1.5× 59 1.2× 44 1.0× 3 674
Yasunori Kitano Japan 13 460 1.4× 180 1.5× 67 1.2× 54 1.1× 43 1.0× 26 598
Cheng Zhu United States 6 438 1.4× 117 1.0× 72 1.3× 29 0.6× 61 1.5× 7 508
Jeffrey L. Havens United States 7 308 1.0× 123 1.0× 21 0.4× 42 0.8× 46 1.1× 10 436
Ulhas P. Dhokte United States 9 437 1.4× 183 1.5× 54 1.0× 69 1.4× 54 1.3× 24 503
William Dent United States 13 445 1.4× 137 1.2× 31 0.6× 26 0.5× 48 1.1× 18 526
Toshiyuki Shimazaki Japan 13 280 0.9× 190 1.6× 27 0.5× 40 0.8× 38 0.9× 27 544
J. L. VAN DER BAAN Netherlands 15 398 1.2× 213 1.8× 91 1.7× 32 0.6× 58 1.4× 49 589

Countries citing papers authored by David M. Hollinshead

Since Specialization
Citations

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

Fields of papers citing papers by David M. Hollinshead

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David M. Hollinshead. 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 David M. Hollinshead. The network helps show where David M. Hollinshead may publish in the future.

Co-authorship network of co-authors of David M. Hollinshead

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

All Works

17 of 17 papers shown
1.
Hollinshead, David M., et al.. (2023). QSP Designer: Quantitative systems pharmacology modeling with modular biological process map notation and multiple language code generation. CPT Pharmacometrics & Systems Pharmacology. 12(7). 889–903. 7 indexed citations
2.
Parker, Seth J., Joel Encarnación-Rosado, Kate E.R. Hollinshead, et al.. (2021). Spontaneous hydrolysis and spurious metabolic properties of α-ketoglutarate esters. Nature Communications. 12(1). 4905–4905. 21 indexed citations
4.
Knight, Julian G., et al.. (2000). Enantioselective Synthesis of 3,6-Dihydro-1H-pyridin-2-ones:  Unexpected Regioselectivity in the Palladium-Catalyzed Decarboxylative Carbonylation of 5-Vinyloxazolidin-2-ones. Journal of the American Chemical Society. 122(12). 2944–2945. 56 indexed citations
5.
Brown, George R., David M. Hollinshead, Elaine S. E. Stokes, et al.. (2000). A Novel Series of 4-Piperidinopyridine and 4-Piperidinopyrimidine Inhibitors of 2,3-Oxidosqualene Cyclase−Lanosterol Synthase. Journal of Medicinal Chemistry. 43(26). 4964–4972. 16 indexed citations
6.
Brown, George R., David M. Hollinshead, Elaine S. E. Stokes, et al.. (1999). Quinuclidine Inhibitors of 2,3-Oxidosqualene Cyclase-Lanosterol Synthase:  Optimization from Lipid Profiles. Journal of Medicinal Chemistry. 42(7). 1306–1311. 16 indexed citations
7.
Markó, István E., Antony Chesney, & David M. Hollinshead. (1994). Asymmetric grignard addition to aldéhydes. An example of inverse temperature dependence of enantiomeric excess.. Tetrahedron Asymmetry. 5(4). 569–572. 10 indexed citations
8.
Ley, Steven V., et al.. (1993). Dispiroketals in Synthesis (Part 3):1Selective Protection of Diequatorial Vicinal Diols in Carbohydrates. Synthesis. 1993(7). 689–692. 15 indexed citations
9.
Morley, Andrew, David M. Hollinshead, & Garry Procter. (1990). Stereoselective cycloadditions of acyl-nitroso compounds; an approach to carbapenem synthesis. Tetrahedron Letters. 31(7). 1047–1050. 15 indexed citations
10.
Hodgson, Simon T., David M. Hollinshead, & Steven V. Ley. (1985). Synthesis of the β-lactam antibiotic (+)- thienamycin via an intermediate π-allyltricarbonyliron lactone complex. Tetrahedron. 41(24). 5871–5878. 21 indexed citations
11.
Hodgson, Simon T., David M. Hollinshead, Steven V. Ley, Caroline M. R. Low, & David J. Williams. (1985). Use of π-allyltricarbonyliron lactam complexes in the preparation of nocardicin derivatives: synthesis of (–)-3-oxo-1-[(p-benzyloxyphenyl)-benzyloxycarbonylmethyl]azetidin-2-one. Journal of the Chemical Society Perkin Transactions 1. 2375–2381. 10 indexed citations
12.
Griffith, William P., et al.. (1984). Oxo complexes of ruthenium(VI) and (VII) as organic oxidants. Journal of the Chemical Society Perkin Transactions 1. 681–686. 74 indexed citations
13.
Hodgson, Simon T., David M. Hollinshead, & Steven V. Ley. (1984). π-Allyltricarbonyliron lactone complexes in synthesis: application to the synthesis of the β-lactam antibiotic (+)-thienamycin. Journal of the Chemical Society Chemical Communications. 494–496. 16 indexed citations
14.
Hollinshead, David M., et al.. (1984). Fe2(co)g in tetrahydrofuran or under sonochemical conditions as convenient practical routes to π-allyltricarbonyliron lactone complexes. Tetrahedron. 40(10). 1737–1742. 29 indexed citations
15.
Annis, Gary D., et al.. (1983). Synthesis of β-lactams from π-allyltricarbonyliron (lactone) complexes. Journal of the Chemical Society Perkin Transactions 1. 2851–2856. 28 indexed citations
16.
Hollinshead, David M., et al.. (1983). The Diels–Alder route to drimane related sesquiterpenes; synthesis of cinnamolide, polygodial, isodrimeninol, drimenin and warburganal. Journal of the Chemical Society Perkin Transactions 1. 1579–1589. 86 indexed citations
17.
Barrett, Anthony G. M., Christopher R. A. Godfrey, David M. Hollinshead, et al.. (1981). Dissolving metal reduction of esters to alkanes. A method for the deoxygenation of alcohols. Journal of the Chemical Society Perkin Transactions 1. 1501–1501. 29 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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