Howard E. Morton

2.9k total citations
53 papers, 1.9k citations indexed

About

Howard E. Morton is a scholar working on Organic Chemistry, Molecular Biology and Biochemistry. According to data from OpenAlex, Howard E. Morton has authored 53 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 44 papers in Organic Chemistry, 17 papers in Molecular Biology and 7 papers in Biochemistry. Recurrent topics in Howard E. Morton's work include Synthetic Organic Chemistry Methods (12 papers), Asymmetric Synthesis and Catalysis (11 papers) and Chemical Synthesis and Reactions (11 papers). Howard E. Morton is often cited by papers focused on Synthetic Organic Chemistry Methods (12 papers), Asymmetric Synthesis and Catalysis (11 papers) and Chemical Synthesis and Reactions (11 papers). Howard E. Morton collaborates with scholars based in United States, Canada and United Kingdom. Howard E. Morton's co-authors include Edward Piers, Christiane Yoakim, John W. Gillard, Yvan Guindon, M. Robert Leanna, A. W. Ford‐Hutchinson, Carol A. Rouzer, J. Michael Chong, Yvan Guindon and Jianguo Ji and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Biological Chemistry and Biochemical and Biophysical Research Communications.

In The Last Decade

Howard E. Morton

52 papers receiving 1.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Howard E. Morton United States 24 1.4k 599 266 262 157 53 1.9k
Dee W. Brooks United States 25 974 0.7× 737 1.2× 338 1.3× 132 0.5× 191 1.2× 56 2.0k
Edward D. Mihelich United States 27 1.3k 1.0× 820 1.4× 228 0.9× 156 0.6× 72 0.5× 46 2.2k
Hiroko Masamune United States 10 1.5k 1.1× 673 1.1× 266 1.0× 208 0.8× 73 0.5× 18 2.1k
K.C. Nicolaou United States 22 1.3k 0.9× 518 0.9× 379 1.4× 79 0.3× 70 0.4× 38 1.8k
David A. Claremon United States 24 992 0.7× 538 0.9× 183 0.7× 101 0.4× 76 0.5× 50 1.7k
Richard W. Friesen Canada 29 1.7k 1.2× 932 1.6× 724 2.7× 104 0.4× 119 0.8× 75 2.5k
W. E. Barnette United States 20 796 0.6× 303 0.5× 283 1.1× 119 0.5× 93 0.6× 36 1.5k
Joseph P. Marino United States 34 2.5k 1.8× 604 1.0× 161 0.6× 245 0.9× 48 0.3× 112 3.2k
Nobuyuki Hamanaka Japan 23 607 0.4× 798 1.3× 335 1.3× 62 0.2× 174 1.1× 119 1.8k
Tuoping Luo China 33 1.8k 1.3× 1.1k 1.9× 314 1.2× 178 0.7× 192 1.2× 65 3.0k

Countries citing papers authored by Howard E. Morton

Since Specialization
Citations

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

Fields of papers citing papers by Howard E. Morton

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Howard E. Morton. 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 Howard E. Morton. The network helps show where Howard E. Morton may publish in the future.

Co-authorship network of co-authors of Howard E. Morton

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

All Works

20 of 20 papers shown
1.
Kerdesky, Francis A. J., M. Robert Leanna, Ji Zhang, et al.. (2006). An Efficient Multikilogram Synthesis of ABT-963:  A Selective COX-2 Inhibitor. Organic Process Research & Development. 10(3). 512–517. 21 indexed citations
2.
Dhaon, Madhup K., et al.. (2006). Synthesis, isolation, and characterization of ABT-578 equilibrium isomers. Tetrahedron Letters. 48(6). 1059–1062. 2 indexed citations
3.
Knutsen, Lars J. S., Knud Erik Andersen, Jesper Lau, et al.. (1999). Synthesis of Novel GABA Uptake Inhibitors. 3. Diaryloxime and Diarylvinyl Ether Derivatives of Nipecotic Acid and Guvacine as Anticonvulsant Agents. Journal of Medicinal Chemistry. 42(18). 3447–3462. 49 indexed citations
4.
Lynch, J.A., Mark W. Holladay, Keith B. Ryther, et al.. (1998). Efficient asymmetric synthesis of ABT-594; a potent, orally effective analgesic. Tetrahedron Asymmetry. 9(16). 2791–2794. 31 indexed citations
5.
Dickman, Daniel A., et al.. (1997). Synthesis of A-79175: a second generation 5-lipoxygenase inhibitor. Tetrahedron Asymmetry. 8(11). 1791–1795. 5 indexed citations
6.
Leanna, M. Robert, Thomas J. Sowin, & Howard E. Morton. (1993). ChemInform Abstract: Synthesis of α‐Amino and α‐Alkoxy Aldehydes via Oxoammonium Oxidation.. ChemInform. 24(2). 3 indexed citations
7.
Kerdesky, Francis A. J., Anthony R. Haight, B. A. Narayanan, et al.. (1993). An Efficient Synthesis of an Angiotensin II Antagonist (A-81988). Synthetic Communications. 23(14). 2027–2039. 8 indexed citations
8.
Leanna, M. Robert, Thomas J. Sowin, & Howard E. Morton. (1992). Synthesis of α-amino and α-alkoxy aldehydes via oxoammonium oxidation. Tetrahedron Letters. 33(35). 5029–5032. 101 indexed citations
9.
DeNinno, Michael P., Richard J. Perner, Howard E. Morton, & Stanley DiDomenico. (1992). The enantioselective synthesis of the potent dopamine D1 agonist (1R,3S)-3-(1'-adamantyl)-1-(aminomethyl)-3,4-dihydro-5,6-dihydroxy-1H-2-benzopyran (A77636). The Journal of Organic Chemistry. 57(26). 7115–7118. 27 indexed citations
10.
Leanna, M. Robert, et al.. (1990). Synthesis of N-(Tert-butoxycarbonyl)-3-(4-thiazoIyl)-L-alanine. Synthetic Communications. 20(22). 3507–3517. 20 indexed citations
11.
Patrignani, Paola, Howard E. Morton, M. Cirino, et al.. (1989). Fractional conversion of thromboxane A2 and B2 to urinary 2,3-dinor-thromboxane B2 and 11-dehydrothromboxane B2 in the cynomolgus monkey. Biochimica et Biophysica Acta (BBA) - General Subjects. 992(1). 71–77. 13 indexed citations
12.
Guindon, Yvan, et al.. (1988). New synthetic applications of dialkylboron halide reagents. Pure and Applied Chemistry. 60(11). 1705–1714. 17 indexed citations
13.
Mayeux, Philip R., Howard E. Morton, John W. Gillard, et al.. (1988). The affinities of prostaglandin H2 and thromboxane A2 for their receptor are similar in washed human platelets. Biochemical and Biophysical Research Communications. 157(2). 733–739. 46 indexed citations
14.
Bernstein, Michael A., Howard E. Morton, & Yvan Guindon. (1986). A general method for determining the anomeric configuration of C-furanoside derivatives: a 1H nuclear magnetic resonance nuclear Overhauser effect study. Journal of the Chemical Society Perkin Transactions 2. 1155–1155. 13 indexed citations
15.
Guindon, Yvan, Christiane Yoakim, & Howard E. Morton. (1984). Dimethylboron bromide and diphenylboron bromide: cleavage of acetals and ketals. The Journal of Organic Chemistry. 49(21). 3912–3920. 136 indexed citations
16.
Piers, Edward, Howard E. Morton, Isao Nagakura, & Richard W. Thies. (1983). Seven-membered ring annulation and spiro-annulation processes via preparation and thermal rearrangement of β-(2-vinylcyclopropyl) α,β-unsaturated ketones. Canadian Journal of Chemistry. 61(6). 1226–1238. 14 indexed citations
17.
18.
Piers, Edward & Howard E. Morton. (1979). .beta.-Acylvinyl anion equivalents: preparation of 1-lithio-3-(tert-butyldimethylsiloxy)-1,3-cyclohexadiene and its reaction with electrophiles. The Journal of Organic Chemistry. 44(19). 3437–3439. 21 indexed citations
19.
Piers, Edward & Howard E. Morton. (1978). Lithium phenylthio(trimethylstannyl)cuprate, a new reagent for conjugate addition of the Me3Sn group. The synthesis of β-trimethylstannyl-αβ-unsaturated ketones. Journal of the Chemical Society Chemical Communications. 1033–1034. 21 indexed citations
20.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Dee W. Brooks Breakdown of academic impact, for papers by Edward D. Mihelich Breakdown of academic impact, for papers by Hiroko Masamune Breakdown of academic impact, for papers by K.C. Nicolaou Breakdown of academic impact, for papers by David A. Claremon Breakdown of academic impact, for papers by Richard W. Friesen Breakdown of academic impact, for papers by W. E. Barnette Breakdown of academic impact, for papers by Joseph P. Marino Breakdown of academic impact, for papers by Nobuyuki Hamanaka Breakdown of academic impact, for papers by Tuoping Luo
Rankless by CCL
2026