Matthew F. Baevsky

569 total citations
7 papers, 451 citations indexed

About

Matthew F. Baevsky is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Matthew F. Baevsky has authored 7 papers receiving a total of 451 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Organic Chemistry, 4 papers in Molecular Biology and 2 papers in Inorganic Chemistry. Recurrent topics in Matthew F. Baevsky's work include Asymmetric Synthesis and Catalysis (3 papers), Cancer therapeutics and mechanisms (2 papers) and Catalytic C–H Functionalization Methods (1 paper). Matthew F. Baevsky is often cited by papers focused on Asymmetric Synthesis and Catalysis (3 papers), Cancer therapeutics and mechanisms (2 papers) and Catalytic C–H Functionalization Methods (1 paper). Matthew F. Baevsky collaborates with scholars based in United States. Matthew F. Baevsky's co-authors include Daniel L. Comins, Hao Hong, Leonard L. Winneroski, Christopher J. Rito, Michael R. Jirousek, William F. Heath, David A. Neel, James R. Gillig, Steven E. Hall and Margaret M. Faul and has published in prestigious journals such as Journal of the American Chemical Society, Journal of Medicinal Chemistry and Tetrahedron.

In The Last Decade

Matthew F. Baevsky

7 papers receiving 435 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Matthew F. Baevsky United States	5	272	188	56	46	41	7	451
David A. Neel United States	9	272 1.0×	189 1.0×	24 0.4×	29 0.6×	39 1.0×	12	479
Ho-Sam Ahn United States	16	287 1.1×	224 1.2×	122 2.2×	16 0.3×	82 2.0×	27	967
Yukiko Honda United States	9	604 2.2×	147 0.8×	62 1.1×	80 1.7×	61 1.5×	12	743
Cécile Gonzalez France	5	272 1.0×	60 0.3×	24 0.4×	22 0.5×	28 0.7×	6	386
Wai C. Wong United States	16	281 1.0×	369 2.0×	26 0.5×	24 0.5×	60 1.5×	29	589
Eleni Gourzoulidou Germany	7	278 1.0×	144 0.8×	17 0.3×	13 0.3×	76 1.9×	9	388
Christina M. Barrett United States	11	160 0.6×	107 0.6×	46 0.8×	19 0.4×	12 0.3×	16	445
Diane R. Sawicki United States	12	374 1.4×	333 1.8×	28 0.5×	82 1.8×	74 1.8×	13	809
Wen‐Zhen Gu United States	14	360 1.3×	221 1.2×	51 0.9×	18 0.4×	21 0.5×	26	686
Colin Howes United Kingdom	9	115 0.4×	103 0.5×	12 0.2×	28 0.6×	75 1.8×	17	406

Countries citing papers authored by Matthew F. Baevsky

Since Specialization

Citations

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

Fields of papers citing papers by Matthew F. Baevsky

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Matthew F. Baevsky

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

All Works

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7 of 7 papers shown

1.

Comins, Daniel L., Paresh Thakker, Matthew F. Baevsky, & Mohamed M. Badawi. (1997). Chiral auxiliary mediated pictet-spengler reactions: Asymmetric syntheses of (−)-laudanosine, (+)-glaucine and (−)-xylopinine. Tetrahedron. 53(48). 16327–16340. 58 indexed citations

2.

Jirousek, Michael R., James R. Gillig, Cécile Gonzalez, et al.. (1996). (S)-13-[(Dimethylamino)methyl]-10,11,14,15-tetrahydro-4,9:16,21-dimetheno- 1H,13H-dibenzo[e,k]pyrrolo[3,4-h][1,4,13]oxadiazacyclohexadecene-1,3(2H)-dione (LY333531) and Related Analogues: Isozyme Selective Inhibitors of Protein Kinase Cβ. Journal of Medicinal Chemistry. 39(14). 2664–2671. 274 indexed citations

3.

Jirousek, Michael R., James R. Gillig, David A. Neel, et al.. (1995). Synthesis of bisindolylmaleimide macrocycles. Bioorganic & Medicinal Chemistry Letters. 5(18). 2093–2096. 12 indexed citations

4.

Comins, Daniel L., Matthew F. Baevsky, & Hao Hong. (1993). ChemInform Abstract: A 10‐Step, Asymmetric Synthesis of (S)‐Camptothecin.. ChemInform. 24(18). 1 indexed citations

5.

Comins, Daniel L., Matthew F. Baevsky, & Hao Hong. (1992). A 10-step, asymmetric synthesis of (S)-camptothecin. Journal of the American Chemical Society. 114(27). 10971–10972. 99 indexed citations

6.

Hill, Richard K., et al.. (1990). A New Route to 1,3-Dienes: TMSI Elimination of 2-Ene-1,4-diols. Synthetic Communications. 20(12). 1877–1884. 4 indexed citations

7.

Baevsky, Matthew F., et al.. (1989). Palladium phosphine catalyzed hydroesterifications of unsaturated nitrogen heterocycles. Journal of Molecular Catalysis. 53(2). 179–192. 3 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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