William P. Malachowski

2.3k total citations · 1 hit paper
34 papers, 1.8k citations indexed

About

William P. Malachowski is a scholar working on Organic Chemistry, Molecular Biology and Biological Psychiatry. According to data from OpenAlex, William P. Malachowski has authored 34 papers receiving a total of 1.8k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Organic Chemistry, 18 papers in Molecular Biology and 12 papers in Biological Psychiatry. Recurrent topics in William P. Malachowski's work include Tryptophan and brain disorders (12 papers), Asymmetric Synthesis and Catalysis (9 papers) and Chemical Synthesis and Analysis (5 papers). William P. Malachowski is often cited by papers focused on Tryptophan and brain disorders (12 papers), Asymmetric Synthesis and Catalysis (9 papers) and Chemical Synthesis and Analysis (5 papers). William P. Malachowski collaborates with scholars based in United States. William P. Malachowski's co-authors include Alexander J. Muller, George C. Prendergast, James B. DuHadaway, James K. Coward, Arpita Mondal, Peggy Scherle, Judith M. LaLonde, Sanjeev Kumar, Paul Gaspari and Tinku Banerjee and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and Cancer Research.

In The Last Decade

William P. Malachowski

34 papers receiving 1.8k 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.

Discovery of IDO1 Inhibitors: From Bench to Bedside

2017 428 citations George C. Prendergast, William P. Malachowski et al. Cancer Research profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
William P. Malachowski United States	19	740	714	486	382	320	34	1.8k
Pierre Larrieu France	11	726 1.0×	535 0.7×	132 0.3×	362 0.9×	288 0.9×	16	1.3k
Raphaël Frédérick Belgium	27	568 0.8×	1.2k 1.7×	703 1.4×	254 0.7×	233 0.7×	80	2.5k
Eddy W. Yue United States	18	303 0.4×	658 0.9×	578 1.2×	217 0.6×	131 0.4×	27	1.3k
Eduard Dolušić Belgium	11	502 0.7×	347 0.5×	153 0.3×	157 0.4×	203 0.6×	15	1.0k
Andrew P. Combs United States	25	320 0.4×	1.7k 2.3×	2.4k 5.0×	377 1.0×	139 0.4×	65	3.9k
Chunxiang Kuang China	31	348 0.5×	528 0.7×	1.7k 3.6×	131 0.3×	163 0.5×	101	2.4k
Alban J. Allentoff United States	15	111 0.1×	344 0.5×	150 0.3×	104 0.3×	55 0.2×	36	845
Xuebin Liao China	29	62 0.1×	581 0.8×	2.0k 4.1×	152 0.4×	32 0.1×	76	2.9k
Josephine S. Modica-Napolitano United States	20	91 0.1×	1.4k 2.0×	202 0.4×	54 0.1×	105 0.3×	25	2.3k
Leggy A. Arnold United States	32	83 0.1×	1.3k 1.9×	1.9k 4.0×	52 0.1×	37 0.1×	114	3.6k

Countries citing papers authored by William P. Malachowski

Since Specialization

Citations

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

Fields of papers citing papers by William P. Malachowski

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by William P. Malachowski. 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 William P. Malachowski. The network helps show where William P. Malachowski may publish in the future.

Co-authorship network of co-authors of William P. Malachowski

This figure shows the co-authorship network connecting the top 25 collaborators of William P. Malachowski. A scholar is included among the top collaborators of William P. Malachowski 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 William P. Malachowski. William P. Malachowski 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

Malachowski, William P., et al.. (2022). Catalytic Enantioselective Birch–Heck Sequence for the Synthesis of Phenanthridinone Derivatives with an All-Carbon Quaternary Stereocenter. The Journal of Organic Chemistry. 87(2). 1154–1172. 1 indexed citations

DuHadaway, James B., Khoa Pham, Ariel Lewis-Ballester, et al.. (2018). Diaryl hydroxylamines as pan or dual inhibitors of indoleamine 2,3-dioxygenase-1, indoleamine 2,3-dioxygenase-2 and tryptophan dioxygenase. European Journal of Medicinal Chemistry. 162. 455–464. 42 indexed citations

Prendergast, George C., William P. Malachowski, Arpita Mondal, Peggy Scherle, & Alexander J. Muller. (2017). Indoleamine 2,3-Dioxygenase and Its Therapeutic Inhibition in Cancer. International review of cell and molecular biology. 336. 175–203. 225 indexed citations

Malachowski, William P., James B. DuHadaway, Ariel Lewis-Ballester, et al.. (2015). O-alkylhydroxylamines as rationally-designed mechanism-based inhibitors of indoleamine 2,3-dioxygenase-1. European Journal of Medicinal Chemistry. 108. 564–576. 33 indexed citations

Malachowski, William P., et al.. (2015). The first report of Lewis acid reagents in the intramolecular Rauhut–Currier reaction. Tetrahedron Letters. 56(44). 6073–6076. 5 indexed citations

LaLonde, Judith M., et al.. (2013). The Tumor-Selective Cytotoxic Agent β-Lapachone is a Potent Inhibitor of IDO1. SHILAP Revista de lepidopterología. 6. 35–45. 24 indexed citations

Kumar, Sanjeev, William P. Malachowski, James B. DuHadaway, et al.. (2008). Indoleamine 2,3-Dioxygenase Is the Anticancer Target for a Novel Series of Potent Naphthoquinone-Based Inhibitors. Journal of Medicinal Chemistry. 51(22). 7325–7325. 5 indexed citations

Muller, Alexander J., James B. DuHadaway, Tinku Banerjee, et al.. (2007). Brassinin compounds exhibit anti-cancer activity mediated through inhibition of the immunotolerogenic enzyme Indoleamine 2,3-dioxygenase (IDO). Cancer Research. 67. 224–224. 1 indexed citations

Banerjee, Tinku, James B. DuHadaway, Paul Gaspari, et al.. (2007). A key in vivo antitumor mechanism of action of natural product-based brassinins is inhibition of indoleamine 2,3-dioxygenase. Oncogene. 27(20). 2851–2857. 150 indexed citations

10.

Paul, Tapas, William P. Malachowski, & Jisun Lee. (2007). Exploration of the Enantioselective Birch−Cope Sequence for the Synthesis of Carbocyclic Quaternary Stereocenters. The Journal of Organic Chemistry. 72(3). 930–937. 14 indexed citations

11.

Paul, Tapas, William P. Malachowski, & Jisun Lee. (2006). The Enantioselective Birch−Cope Sequence for the Synthesis of Carbocyclic Quaternary Stereocenters. Application to the Synthesis of (+)-Mesembrine. Organic Letters. 8(18). 4007–4010. 32 indexed citations

12.

Wang, Bei, et al.. (2005). A general strategy for the synthesis of azapeptidomimetic lactams. Tetrahedron. 61(43). 10277–10284. 19 indexed citations

13.

Malachowski, William P., et al.. (2005). A new cancer immunosuppression target: Indoleamine 2,3-dioxygenase(IDO). A review of the IDO mechanism, inhibition and therapeuticapplications. Drugs of the Future. 30(9). 897–897. 3 indexed citations

14.

Malachowski, William P., et al.. (2004). Sequential Birch reduction–allylation and Cope rearrangement of o-anisic acid derivatives. Tetrahedron Letters. 45(44). 8183–8185. 3 indexed citations

15.

Malachowski, William P., et al.. (2002). The Synthesis of Azapeptidomimetic β-Lactam Molecules as Potential Protease Inhibitors. The Journal of Organic Chemistry. 67(25). 8962–8969. 29 indexed citations

16.

Schultz, Arthur G., et al.. (1997). Asymmetric Total Synthesis of (+)-Apovincamine and a Formal Synthesis of (+)-Vincamine. Demonstration of a Practical “Asymmetric Linkage” between Aromatic Carboxylic Acids and Chiral Acyclic Substrates. The Journal of Organic Chemistry. 62(5). 1223–1229. 35 indexed citations

17.

Malachowski, William P. & James K. Coward. (1995). ChemInform Abstract: The Chemistry of Phosphapeptides: Investigations on the Synthesis of Phosphonamidate, Phosphonate, and Phosphinate Analogues of Glutamyl‐. gamma.‐glutamate.. ChemInform. 26(25). 4 indexed citations

18.

Malachowski, William P., et al.. (1994). Nature of the rate-determining steps of the reaction catalyzed by the Yersinia protein-tyrosine phosphatase.. Journal of Biological Chemistry. 269(11). 8140–8145. 74 indexed citations

19.

Malachowski, William P. & James K. Coward. (1994). The Chemistry of Phosphapeptides: Formation of Functionalized Phosphonochloridates under Mild Conditions and Their Reaction with Alcohols and Amines. The Journal of Organic Chemistry. 59(25). 7616–7624. 55 indexed citations

20.

Malachowski, William P. & James K. Coward. (1994). The Chemistry of Phosphapeptides: Investigations on the Synthesis of Phosphonamidate, Phosphonate, and Phosphinate Analogs of Glutamyl-.gamma.-glutamate. The Journal of Organic Chemistry. 59(25). 7625–7634. 64 indexed citations

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