Matthew J. Hesse

1.2k total citations · 1 hit paper
17 papers, 598 citations indexed

About

Matthew J. Hesse is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Matthew J. Hesse has authored 17 papers receiving a total of 598 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Organic Chemistry, 4 papers in Molecular Biology and 3 papers in Pharmacology. Recurrent topics in Matthew J. Hesse's work include Organoboron and organosilicon chemistry (6 papers), Asymmetric Synthesis and Catalysis (5 papers) and Advanced Synthetic Organic Chemistry (5 papers). Matthew J. Hesse is often cited by papers focused on Organoboron and organosilicon chemistry (6 papers), Asymmetric Synthesis and Catalysis (5 papers) and Advanced Synthetic Organic Chemistry (5 papers). Matthew J. Hesse collaborates with scholars based in United Kingdom, United States and France. Matthew J. Hesse's co-authors include Varinder K. Aggarwal, Christine L. Willis, Craig P. Butts, Jack L.‐Y. Chen, Helen K. Scott, Eddie L. Myers, James R. Smith, Beatrice S. L. Collins, M. A. Graham and David J. Hirst and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

Matthew J. Hesse

17 papers receiving 593 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Rational Chemical Design of Molecular Glue Degraders

2023 103 citations Ethan S. Toriki, James W. Papatzimas et al. ACS Central Science profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Matthew J. Hesse United Kingdom	10	459	204	98	47	32	17	598
Said Elgendy United Kingdom	14	429 0.9×	122 0.6×	65 0.7×	65 1.4×	35 1.1×	23	530
Sylvain Collet France	15	422 0.9×	189 0.9×	107 1.1×	32 0.7×	19 0.6×	36	544
Klement Foo United States	12	779 1.7×	182 0.9×	93 0.9×	42 0.9×	63 2.0×	16	890
Subham Mahapatra United States	14	489 1.1×	159 0.8×	79 0.8×	16 0.3×	80 2.5×	23	578
Aneta Turlik United States	14	454 1.0×	181 0.9×	161 1.6×	14 0.3×	17 0.5×	25	559
Heather Burks United States	8	983 2.1×	273 1.3×	318 3.2×	37 0.8×	22 0.7×	10	1.1k
Chunngai Hui China	13	444 1.0×	141 0.7×	102 1.0×	19 0.4×	43 1.3×	18	562
Guangjun Bao China	15	504 1.1×	188 0.9×	72 0.7×	20 0.4×	32 1.0×	32	569
Roxanne K. Kunz United States	10	580 1.3×	162 0.8×	64 0.7×	14 0.3×	22 0.7×	13	662
Sushant Malhotra United States	14	736 1.6×	126 0.6×	233 2.4×	17 0.4×	32 1.0×	29	821

Countries citing papers authored by Matthew J. Hesse

Since Specialization

Citations

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

Fields of papers citing papers by Matthew J. Hesse

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Matthew J. Hesse. 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 Matthew J. Hesse. The network helps show where Matthew J. Hesse may publish in the future.

Co-authorship network of co-authors of Matthew J. Hesse

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

All Works

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17 of 17 papers shown

1.

Taft, Benjamin R., Matthew J. Hesse, Mulugeta Mamo, et al.. (2025). Discovery and Optimization of a Novel Series of Influenza A Virus Replication Inhibitors Targeting the Nucleoprotein Protein–Protein Interaction. Journal of Medicinal Chemistry. 68(15). 16349–16370. 1 indexed citations

2.

Forte, Nafsika, Dustin Dovala, Matthew J. Hesse, et al.. (2023). Targeted Protein Degradation through E2 Recruitment. ACS Chemical Biology. 18(4). 897–904. 33 indexed citations

3.

Toriki, Ethan S., James W. Papatzimas, Dustin Dovala, et al.. (2023). Rational Chemical Design of Molecular Glue Degraders. ACS Central Science. 9(5). 915–926. 103 indexed citations breakdown →

4.

Hesse, Matthew J., et al.. (2020). A copper-catalyzed asymmetric oxime propargylation enables the synthesis of the gliovirin tetrahydro-1,2-oxazine core. Chemical Science. 11(43). 11897–11901. 7 indexed citations

5.

Smith, James R., Beatrice S. L. Collins, Matthew J. Hesse, et al.. (2017). Enantioselective Rhodium(III)-Catalyzed Markovnikov Hydroboration of Unactivated Terminal Alkenes. Journal of the American Chemical Society. 139(27). 9148–9151. 106 indexed citations

6.

Blair, Daniel J., et al.. (2016). Full chirality transfer in the synthesis of hindered tertiary boronic esters under in situ lithiation–borylation conditions. Chemical Communications. 52(30). 5289–5292. 8 indexed citations

7.

Hesse, Matthew J., Stéphanie Essafi, Jeremy N. Harvey, et al.. (2014). Highly Selective Allylborations of Aldehydes Using α,α‐Disubstituted Allylic Pinacol Boronic Esters. Angewandte Chemie. 126(24). 6259–6263. 22 indexed citations

8.

Hesse, Matthew J., Stéphanie Essafi, Jeremy N. Harvey, et al.. (2014). Highly Selective Allylborations of Aldehydes Using α,α‐Disubstituted Allylic Pinacol Boronic Esters. Angewandte Chemie International Edition. 53(24). 6145–6149. 54 indexed citations

9.

Chen, Jack L.‐Y., Helen K. Scott, Matthew J. Hesse, Christine L. Willis, & Varinder K. Aggarwal. (2013). Highly Diastereo- and Enantioselective Allylboration of Aldehydes using α-Substituted Allyl/Crotyl Pinacol Boronic Esters via in Situ Generated Borinic Esters. Journal of the American Chemical Society. 135(14). 5316–5319. 111 indexed citations

10.

Aggarwal, Varinder K., Liam T. Ball, Matthew J. Hesse, et al.. (2012). Application of the lithiation–borylation reaction to the rapid and enantioselective synthesis of the bisabolane family of sesquiterpenes. Chemical Communications. 48(74). 9230–9230. 29 indexed citations

11.

Hesse, Matthew J., Craig P. Butts, Christine L. Willis, & Varinder K. Aggarwal. (2012). Diastereodivergent Synthesis of Trisubstituted Alkenes through Protodeboronation of Allylic Boronic Esters: Application to the Synthesis of the Californian Red Scale Beetle Pheromone. Angewandte Chemie International Edition. 51(50). 12444–12448. 69 indexed citations

12.

Hesse, Matthew J., Craig P. Butts, Christine L. Willis, & Varinder K. Aggarwal. (2012). Diastereodivergent Synthesis of Trisubstituted Alkenes through Protodeboronation of Allylic Boronic Esters: Application to the Synthesis of the Californian Red Scale Beetle Pheromone. Angewandte Chemie. 124(50). 12612–12616. 23 indexed citations

13.

Linden, Anthony, et al.. (1998). AmaryllidaceaeAlkaloids: (+)-Tazettine, (+)-3-O-Demethylcriwelline and (+)-3-Epimacronine at 173 K. Acta Crystallographica Section C Crystal Structure Communications. 54(11). 1653–1659. 6 indexed citations

14.

Hesse, Matthew J., et al.. (1998). ChemInform Abstract: The Gracilines: A Novel Subgroup of the Amaryllidaceae Alkaloids.. ChemInform. 29(51). 2 indexed citations

15.

Borris, Robert P., Karin Seifert, S. Johne, & Matthew J. Hesse. (1983). ChemInform Abstract: 2‐(6′‐(O‐TRANS‐CINNAMOYL)‐β‐D‐GLUCOPYRANOSYLOXY))‐3‐METHYL‐4H‐PYRAN‐4‐ONE, A NEW ACYLATED PYRONE GLUCOSIDE FROM SILENE VULGARIS (CARYOPHYLLACEAE). Chemischer Informationsdienst. 14(14). 1 indexed citations

16.

Hesse, Matthew J., et al.. (1981). ChemInform Abstract: MASS SPECTROMETRIC STUDIES. PART 36. MASS SPECTROMETRIC DECOMPOSITION OF MONOHALOGENATED ACETIC ACIDS AND ESTERS. Chemischer Informationsdienst. 12(45). 1 indexed citations

17.

Kompiš, I., Matthew J. Hesse, & Helmut Schmid. (1971). An approach to the biogenetic classification of indole alkaloids.. PubMed. 34(3). 269–91. 22 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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