David Lathbury

791 total citations
27 papers, 571 citations indexed

About

David Lathbury is a scholar working on Organic Chemistry, Pharmaceutical Science and Inorganic Chemistry. According to data from OpenAlex, David Lathbury has authored 27 papers receiving a total of 571 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Organic Chemistry, 4 papers in Pharmaceutical Science and 4 papers in Inorganic Chemistry. Recurrent topics in David Lathbury's work include Asymmetric Synthesis and Catalysis (11 papers), Synthetic Organic Chemistry Methods (10 papers) and Catalytic Alkyne Reactions (7 papers). David Lathbury is often cited by papers focused on Asymmetric Synthesis and Catalysis (11 papers), Synthetic Organic Chemistry Methods (10 papers) and Catalytic Alkyne Reactions (7 papers). David Lathbury collaborates with scholars based in United Kingdom, United States and Netherlands. David Lathbury's co-authors include Timothy Gallagher, Kieran C. Molloy, Philip J. Parsons, David Fox, R.G. Kinsman, Ivan L. Pinto, Robert W. Shaw, Mary F. Mahon, Philip C. Bulman Page and Mary F. Mahon and has published in prestigious journals such as Journal of the American Chemical Society, Tetrahedron and Tetrahedron Letters.

In The Last Decade

David Lathbury

26 papers receiving 529 citations

Peers

David Lathbury

PHARM

Moncef Bellassoued France

Masashige Yamauchi Japan

M. Rambaud France

Nigel Hussain United Kingdom

Sajan P. Joseph United States

Darren Stead United Kingdom

Andrzej Leniewski Poland

M. Nagarajan India

M. T. NUNEZ Spain

Andreas Job Germany

Moncef Bellassoued France

David Lathbury

530 ×1.0

89 ×0.9

50 ×0.5

31 ×1.2

25 ×1.1

PHARM

Citations per year, relative to David Lathbury David Lathbury (= 1×) peers Moncef Bellassoued

Countries citing papers authored by David Lathbury

Since Specialization

Citations

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

Fields of papers citing papers by David Lathbury

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of David Lathbury

This figure shows the co-authorship network connecting the top 25 collaborators of David Lathbury. A scholar is included among the top collaborators of David Lathbury 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 Lathbury. David Lathbury 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

Lathbury, David. (2006). SPECIAL FEATURE SECTION: SOLVENTS AND SOLVENT EFFECTS. Organic Process Research & Development. 11(1). 104–104. 1 indexed citations

Karl, W., Richard K. Bellingham, David S. Ennis, et al.. (2001). Development of an Efficient and Stereoselective Manufacturing Route to Idoxifene. Organic Process Research & Development. 5(5). 479–490. 14 indexed citations

Ennis, David S., et al.. (1998). Scale-Up of an Intermolecular Barbier Reaction. Organic Process Research & Development. 2(5). 287–289. 4 indexed citations

Page, Philip C. Bulman, et al.. (1997). Regioselective and stereoselective 1,3-dipolar addition of nitrile oxides to 2--crotyl-1,3-dithiane 2-oxides. Tetrahedron. 53(3). 1061–1080. 12 indexed citations

Szeto, Peter, et al.. (1997). Oxazaborolidine-mediated reduction of prochiral 2-alkylidene cycloalkanones. Tetrahedron Asymmetry. 8(5). 673–676. 13 indexed citations

Stockman, Robert A., Peter Szeto, Stephen Thompson, et al.. (1996). Synthesis of Functionalised Azabicycles via a Regiospecific Intramolecular Aldol Reaction. Synlett. 1996(9). 853–855. 6 indexed citations

Page, Philip C. Bulman, Mark Purdie, & David Lathbury. (1996). Enantioselective synthesis of α-hydroxyketones using the ditox asymmetric building block. Tetrahedron Letters. 37(49). 8929–8932. 13 indexed citations

Szeto, Peter, David Lathbury, & Timothy Gallagher. (1995). Heterocyclic ketones as pre-formed building blocks. Synthesis of (−)-slaframine. Tetrahedron Letters. 36(38). 6957–6960. 14 indexed citations

Lathbury, David, et al.. (1995). Preparation of 2-aryl and 2-heteroaryl substituted penems by palladium mediated cross coupling. Tetrahedron Letters. 36(5). 775–776. 9 indexed citations

10.

Hussain, Nigel, et al.. (1995). Synthesis of an α-(aminooxy)arylacetic ester by the reaction of an α-diazo ester with n-hydroxyphthalimide. Tetrahedron Letters. 36(44). 8141–8144. 6 indexed citations

11.

Fox, David, David Lathbury, Mary F. Mahon, Kieran C. Molloy, & Timothy Gallagher. (1991). Enantioselective synthesis of pumiliotoxin 251D. A strategy employing an allene-based electrophile-mediated cyclization. Journal of the American Chemical Society. 113(7). 2652–2656. 71 indexed citations

12.

Huby, Nicholas, et al.. (1991). Synthetic and stereochemical studies directed towards anatoxin-a. Journal of the Chemical Society Perkin Transactions 1. 145–145. 16 indexed citations

13.

Fox, David, David Lathbury, Mary F. Mahon, Kieran C. Molloy, & Timothy Gallagher. (1989). Asymmetric synthesis of functionalised pyrrolidines. The role of a stereogenic centre on nitrogen. Journal of the Chemical Society Chemical Communications. 1073–1073. 33 indexed citations

14.

Lathbury, David, et al.. (1989). Electrophile-mediated cyclisations: regioselective synthesis of substituted cyclic nitrones and crystal structures of the nitrone cycloadducts. Journal of the Chemical Society Perkin Transactions 1. 2415–2415. 33 indexed citations

15.

Lathbury, David, Philip J. Parsons, & Ivan L. Pinto. (1988). A route to the pyrrolizidine ring system using a novel radical cyclisation. Journal of the Chemical Society Chemical Communications. 81–81. 55 indexed citations

16.

Kinsman, R.G., et al.. (1987). Stereoselectivity in the synthesis of 2,5-disubstituted pyrrolidines. Journal of the Chemical Society Chemical Communications. 243–243. 62 indexed citations

17.

Lathbury, David & Timothy Gallagher. (1986). Stereoselective synthesis of pyrrolizidine alkaloids via substituted nitrones. Journal of the Chemical Society Chemical Communications. 1017–1017. 29 indexed citations

18.

Lathbury, David, et al.. (1986). Palladium(II)-mediated routes to functionalised heterocycles. Tetrahedron Letters. 27(49). 6009–6012. 46 indexed citations

19.

Lathbury, David & Timothy Gallagher. (1985). A new approach to cyclic nitrones: Application to the synthesis of α,α′-disubstituted piperidines and pyrrolidines. Tetrahedron Letters. 26(50). 6249–6252. 25 indexed citations

20.

Lathbury, David & Philip J. Parsons. (1982). Studies on the addition of nitrile oxides to 1-phenylthiobuta-1,3-diene, a new directed aldol condensation. Journal of the Chemical Society Chemical Communications. 291–291. 11 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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