Peter G. Houghton

485 total citations
18 papers, 369 citations indexed

About

Peter G. Houghton is a scholar working on Organic Chemistry, Pharmacology and Molecular Biology. According to data from OpenAlex, Peter G. Houghton has authored 18 papers receiving a total of 369 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Organic Chemistry, 7 papers in Pharmacology and 4 papers in Molecular Biology. Recurrent topics in Peter G. Houghton's work include Synthesis of Organic Compounds (5 papers), Click Chemistry and Applications (2 papers) and Chemical Synthesis and Analysis (2 papers). Peter G. Houghton is often cited by papers focused on Synthesis of Organic Compounds (5 papers), Click Chemistry and Applications (2 papers) and Chemical Synthesis and Analysis (2 papers). Peter G. Houghton collaborates with scholars based in United Kingdom and United States. Peter G. Houghton's co-authors include H. Suschitzky, A. O. FITTON, Stanley H. B. Wright, Ian F. Cottrell, Guy R. Humphrey, Robert A. Reamer, Paul J. Reider, Charles W. Rees, Michael S. Ashwood and David Lieberman and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Journal of Pharmaceutical Sciences.

In The Last Decade

Peter G. Houghton

18 papers receiving 349 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Peter G. Houghton United Kingdom 13 308 87 86 24 20 18 369
Jean Marie Beau United States 6 391 1.3× 125 1.4× 77 0.9× 22 0.9× 35 1.8× 7 498
Édouard Untersteller United States 8 287 0.9× 89 1.0× 80 0.9× 11 0.5× 16 0.8× 9 355
Leonardo Di Nunno Italy 13 380 1.2× 155 1.8× 70 0.8× 18 0.8× 34 1.7× 46 481
Marvin P. Cohen United States 12 243 0.8× 62 0.7× 90 1.0× 24 1.0× 31 1.6× 21 333
V. SPEZIALE France 10 236 0.8× 86 1.0× 47 0.5× 13 0.5× 31 1.6× 36 306
Keith E. McCarthy United States 11 341 1.1× 137 1.6× 48 0.6× 11 0.5× 18 0.9× 19 401
F. P. J. T. Rutjes United States 5 292 0.9× 64 0.7× 84 1.0× 9 0.4× 16 0.8× 6 345
F. FARINA Spain 13 427 1.4× 75 0.9× 54 0.6× 43 1.8× 29 1.4× 55 529
Shin Chung South Korea 9 275 0.9× 95 1.1× 94 1.1× 30 1.3× 42 2.1× 17 364
Kevin E. Henegar United States 12 267 0.9× 137 1.6× 36 0.4× 16 0.7× 19 0.9× 20 372

Countries citing papers authored by Peter G. Houghton

Since Specialization
Citations

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

Fields of papers citing papers by Peter G. Houghton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Peter G. Houghton. 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 Peter G. Houghton. The network helps show where Peter G. Houghton may publish in the future.

Co-authorship network of co-authors of Peter G. Houghton

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

All Works

18 of 18 papers shown
1.
Kopach, Michael E., et al.. (2015). Practical Asymmetric Synthesis of an Edivoxetine·HCl Intermediate via an Efficient Diazotization Process. Organic Process Research & Development. 19(4). 543–550. 7 indexed citations
2.
Baertschi, Steven W., Patrick J. Jansen, William K. Smith, et al.. (2014). Investigation of the Mechanism of Racemization of Litronesib in Aqueous Solution: Unexpected Base‐Catalyzed Inversion of a Fully Substituted Carbon Chiral Center. Journal of Pharmaceutical Sciences. 103(9). 2797–2808. 5 indexed citations
3.
4.
Williams, J. Michael, Karel M. J. Brands, Renato T. Skerlj, et al.. (2005). Practical Synthesis of the New Carbapenem Antibiotic Ertapenem Sodium. The Journal of Organic Chemistry. 70(19). 7479–7487. 15 indexed citations
5.
Brands, Karel M. J., Ronald B. Jobson, Karen M. Conrad, et al.. (2002). Efficient One-Pot Synthesis of the 2-Aminocarbonylpyrrolidin-4-ylthio-Containing Side Chain of the New Broad-Spectrum Carbapenem Antibiotic Ertapenem. The Journal of Organic Chemistry. 67(14). 4771–4776. 18 indexed citations
6.
Maligres, Peter E., Ioannis N. Houpis, Kai Rossen, et al.. (1997). Synthesis of the orally active spiroindoline-based growth hormone secretagogue, MK-677. Tetrahedron. 53(32). 10983–10992. 41 indexed citations
7.
Ashwood, Michael S., et al.. (1995). Synthesis of the selective muscarinic agonist (3R)-3-(6-chloropyrazin-2-yl)-1-azabicyclo [2.2.2] octane. Journal of the Chemical Society Perkin Transactions 1. 641–641. 13 indexed citations
8.
Lieberman, David, Robert D. Larsen, Robert A. Reamer, et al.. (1994). Synthesis of the 5-HT1D receptor agonist MK-0462 via a Pd-catalyzed coupling reaction. Tetrahedron Letters. 35(38). 6981–6984. 66 indexed citations
9.
Houghton, Peter G., et al.. (1993). Enantiospecific synthesis of the (4R)-1-azabicyclo[2.2.1]heptane ring system. Journal of the Chemical Society Perkin Transactions 1. 1421–1421. 15 indexed citations
10.
Cottrell, Ian F., et al.. (1991). An improved procedure for the preparation of 1‐benzyl‐1H‐1,2,3‐triazoles from benzyl azides. Journal of Heterocyclic Chemistry. 28(2). 301–304. 41 indexed citations
11.
Ashwood, Michael S., et al.. (1989). Synthesis of 5,6-dihydro-4H-imidazo[1,5-a][4,1]benzoxazepin-6-ones and their transformation into 5,6-dihydro-4H-imidazo[1,5-a][1,4]benzodiazepin-6-ones. Journal of the Chemical Society Perkin Transactions 1. 1889–1889. 2 indexed citations
12.
Ashwood, Michael S., et al.. (1988). Synthesis of 1,1-Diaryl-2,2-dimethoxyethanes. Synthesis. 1988(5). 379–381. 21 indexed citations
13.
Houghton, Peter G., et al.. (1985). Intramolecular reaction between nitro and carbodi-imide groups; a new synthesis of 2-arylbenzotriazoles. Journal of the Chemical Society Perkin Transactions 1. 1471–1471. 30 indexed citations
14.
FITTON, A. O., et al.. (1979). Reactions of formylchromone derivatives. Part 2. Addition reactions of 3-(aryliminomethyl)chromones. Journal of the Chemical Society Perkin Transactions 1. 1691–1691. 26 indexed citations
15.
Houghton, Peter G., et al.. (1979). A new nitro group interaction: conversion of o-nitrophenylcarbodi-imides into benzotriazoles. Journal of the Chemical Society Chemical Communications. 771–771. 7 indexed citations
16.
FITTON, A. O., Peter G. Houghton, & H. Suschitzky. (1979). Reactions of Formylchromone Derivatives; 31. A Facile Synthesis of Fused Benzopyrano-benzothiazepinones, -benzoxazepinones, and -benzodiazepinones. Synthesis. 1979(5). 337–339. 26 indexed citations
17.
FITTON, A. O., et al.. (1977). Conversion of 3-Formylchromones into Pyrrole and Thiophene Derivatives. Synthesis. 1977(2). 133–135. 20 indexed citations
18.
FITTON, A. O., et al.. (1977). Reactions of formylchromone derivatives. Part 1. Cycloadditions to 2- and 3-(aryliminomethyl)chromones. Journal of the Chemical Society Perkin Transactions 1. 1450–1450. 14 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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