I. M. HELPS

405 total citations
9 papers, 340 citations indexed

About

I. M. HELPS is a scholar working on Organic Chemistry, Radiology, Nuclear Medicine and Imaging and Molecular Biology. According to data from OpenAlex, I. M. HELPS has authored 9 papers receiving a total of 340 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Organic Chemistry, 4 papers in Radiology, Nuclear Medicine and Imaging and 3 papers in Molecular Biology. Recurrent topics in I. M. HELPS's work include Chemical Synthesis and Analysis (3 papers), Radiopharmaceutical Chemistry and Applications (3 papers) and Metal complexes synthesis and properties (3 papers). I. M. HELPS is often cited by papers focused on Chemical Synthesis and Analysis (3 papers), Radiopharmaceutical Chemistry and Applications (3 papers) and Metal complexes synthesis and properties (3 papers). I. M. HELPS collaborates with scholars based in United Kingdom, United States and Canada. I. M. HELPS's co-authors include David Parker, James Chapman, David C. Billington, J. Richard Morphy, Peter L. Pauson, Debra Willison, George Ferguson, Andrew S. Craig, Karl J. Jankowski and Byron A. Boyce and has published in prestigious journals such as Tetrahedron, Journal of Organometallic Chemistry and Polyhedron.

In The Last Decade

I. M. HELPS

9 papers receiving 310 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
I. M. HELPS United Kingdom 8 175 121 103 93 66 9 340
Steven R. Woulfe United States 11 166 0.9× 139 1.1× 102 1.0× 42 0.5× 128 1.9× 15 437
Karl J. Jankowski United Kingdom 9 86 0.5× 204 1.7× 102 1.0× 95 1.0× 68 1.0× 12 331
Katrina S. Woodin United States 7 103 0.6× 207 1.7× 97 0.9× 153 1.6× 62 0.9× 7 390
P. Leibnitz Germany 14 195 1.1× 285 2.4× 150 1.5× 182 2.0× 62 0.9× 52 557
Ernest Wong Canada 10 64 0.4× 126 1.0× 135 1.3× 184 2.0× 56 0.8× 10 402
Rebeca G. Balasingham United Kingdom 6 166 0.9× 71 0.6× 172 1.7× 157 1.7× 67 1.0× 6 366
Nathalie Le Bris France 14 207 1.2× 132 1.1× 203 2.0× 111 1.2× 176 2.7× 42 532
Andrew R. Burgoyne South Africa 12 138 0.8× 123 1.0× 71 0.7× 131 1.4× 27 0.4× 19 342
S. Pailloux United States 11 96 0.5× 102 0.8× 181 1.8× 77 0.8× 42 0.6× 21 396
Kevin M. Knopf United States 5 272 1.6× 99 0.8× 111 1.1× 334 3.6× 104 1.6× 8 501

Countries citing papers authored by I. M. HELPS

Since Specialization
Citations

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

Fields of papers citing papers by I. M. HELPS

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of I. M. HELPS

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

All Works

9 of 9 papers shown
2.
HELPS, I. M., David Parker, J. Richard Morphy, & James Chapman. (1989). General routes for the synthesis of mono, di and tri-N-substituted derivatives of cyclam. Tetrahedron. 45(1). 219–226. 72 indexed citations
3.
Craig, Andrew S., I. M. HELPS, David Parker, et al.. (1989). Crystal and molecular structure of a seven-coordinate chloroindium(III) complex of 1,4,7-triazacyclononanetriacetic acid. Polyhedron. 8(20). 2481–2484. 22 indexed citations
4.
HELPS, I. M., et al.. (1989). Syntheses of C- and N-functionalised derivatives of 1,5,9-triazacyclododecane. Journal of the Chemical Society Perkin Transactions 1. 2079–2079. 8 indexed citations
5.
6.
Craig, Andrew S., I. M. HELPS, Karl J. Jankowski, et al.. (1989). Towards tumour imaging with indium-111 labelled macrocycle–antibody conjugates. Journal of the Chemical Society Chemical Communications. 794–796. 40 indexed citations
7.
Billington, David C., et al.. (1988). Synthesis of jasmone, jasmonic acid and some analogues from alkyne-cobalt complexes via the Khand reaction. Journal of Chemical Research Synopses. 1988(10). 326–328. 1 indexed citations
8.
HELPS, I. M., David Parker, James Chapman, & George Ferguson. (1988). Selective N,N-functionalisation of cyclam: crystal structure of the Cu2+ complex of 1,4,8,11-tetra-azacyclotetradecane-1,8-diacetic acid and the tricyclic lactam 15,18-dioxo-1,5,8,12-tetra-azatricyclo[10.2.2.25.8]tetradecane. Journal of the Chemical Society Chemical Communications. 1094–1094. 34 indexed citations
9.
Billington, David C., et al.. (1988). The effect of ultrasound and of phosphine and phosphine-oxides on the Khand reaction. Journal of Organometallic Chemistry. 354(2). 233–242. 89 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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