Yoshito Kishi

20.5k total citations · 4 hit papers
346 papers, 15.2k citations indexed

About

Yoshito Kishi is a scholar working on Organic Chemistry, Molecular Biology and Biotechnology. According to data from OpenAlex, Yoshito Kishi has authored 346 papers receiving a total of 15.2k indexed citations (citations by other indexed papers that have themselves been cited), including 207 papers in Organic Chemistry, 117 papers in Molecular Biology and 59 papers in Biotechnology. Recurrent topics in Yoshito Kishi's work include Synthetic Organic Chemistry Methods (65 papers), Carbohydrate Chemistry and Synthesis (49 papers) and Marine Sponges and Natural Products (48 papers). Yoshito Kishi is often cited by papers focused on Synthetic Organic Chemistry Methods (65 papers), Carbohydrate Chemistry and Synthesis (49 papers) and Marine Sponges and Natural Products (48 papers). Yoshito Kishi collaborates with scholars based in United States, Japan and France. Yoshito Kishi's co-authors include William J. Christ, Jaeho Cha, Osamu Shimomura, Tohru Fukuyama, Hiroto Nagaoka, Jun’ichi Uenishi, Yoshihisa Kobayashi, Jin Kun, Branislav Musicki and Toshio Goto and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Yoshito Kishi

340 papers receiving 14.5k citations

Hit Papers

Highly stereoselective approaches to .alpha.- and .beta.-... 1982 2026 1996 2011 1982 1986 1983 1984 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yoshito Kishi United States 64 10.4k 5.4k 2.4k 2.4k 1.6k 346 15.2k
K. C. Nicolaou United States 62 9.8k 0.9× 3.5k 0.7× 2.1k 0.9× 1.3k 0.5× 844 0.5× 224 12.6k
Stephen Hanessian Canada 65 14.5k 1.4× 9.2k 1.7× 1.9k 0.8× 1.3k 0.5× 275 0.2× 571 19.1k
Henry Rapoport United States 60 7.5k 0.7× 6.0k 1.1× 1.3k 0.5× 617 0.3× 691 0.4× 401 12.8k
Yoel Kashman Israel 48 5.7k 0.5× 4.4k 0.8× 3.6k 1.5× 5.2k 2.1× 523 0.3× 336 13.6k
Masahiro Hirama Japan 50 6.9k 0.7× 2.7k 0.5× 813 0.3× 1.3k 0.5× 2.4k 1.5× 331 9.2k
Jack E. Baldwin United Kingdom 60 11.0k 1.1× 7.8k 1.4× 3.0k 1.2× 1.2k 0.5× 252 0.2× 638 19.0k
Jun’ichi Kobayashi Japan 55 6.1k 0.6× 3.4k 0.6× 3.9k 1.6× 2.3k 1.0× 1.0k 0.6× 424 11.6k
Minoru Isobe Japan 48 5.8k 0.6× 4.3k 0.8× 915 0.4× 1.3k 0.6× 1.7k 1.0× 421 10.2k
Shigeki Matsunaga Japan 51 3.6k 0.3× 3.7k 0.7× 3.5k 1.5× 3.8k 1.6× 602 0.4× 240 9.2k
Scott D. Rychnovsky United States 51 6.8k 0.7× 2.8k 0.5× 1.3k 0.5× 1.4k 0.6× 431 0.3× 218 9.2k

Countries citing papers authored by Yoshito Kishi

Since Specialization
Citations

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

Fields of papers citing papers by Yoshito Kishi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Yoshito Kishi. 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 Yoshito Kishi. The network helps show where Yoshito Kishi may publish in the future.

Co-authorship network of co-authors of Yoshito Kishi

This figure shows the co-authorship network connecting the top 25 collaborators of Yoshito Kishi. A scholar is included among the top collaborators of Yoshito Kishi 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 Yoshito Kishi. Yoshito Kishi 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.
Kishi, Yoshito, et al.. (2024). Application of Ni/Zr-Mediated Ketone Coupling for the Scalable Synthesis of Homohalichondrin B. Organic Letters. 26(34). 7105–7109.
2.
Kishi, Yoshito, et al.. (2020). Total Synthesis of Halistatins 1 and 2. Journal of the American Chemical Society. 142(34). 14743–14749. 13 indexed citations
3.
Yahata, Kenzo, et al.. (2017). Stereocontrolled Synthesis of Left Halves of Halichondrins. The Journal of Organic Chemistry. 82(17). 8808–8830. 9 indexed citations
4.
Yahata, Kenzo, et al.. (2017). Unified Synthesis of Right Halves of Halichondrins A–C. The Journal of Organic Chemistry. 82(17). 8792–8807. 7 indexed citations
5.
Yahata, Kenzo, et al.. (2017). Fe/Cu-Mediated One-Pot Ketone Synthesis. Organic Letters. 19(10). 2766–2769. 21 indexed citations
6.
Lee, Jung Hwa, et al.. (2016). Extension of Pd-Mediated One-Pot Ketone Synthesis to Macrocyclization: Application to a New Convergent Synthesis of Eribulin. Journal of the American Chemical Society. 138(50). 16248–16251. 15 indexed citations
7.
Towle, Murray J., K. Nomoto, Makoto Asano, et al.. (2012). Broad spectrum preclinical antitumor activity of eribulin (Halaven(R)): optimal effectiveness under intermittent dosing conditions.. PubMed. 32(5). 1611–9. 38 indexed citations
8.
Shan, Mingde & Yoshito Kishi. (2012). Concise and Highly Stereoselective Synthesis of the C20–C26 Building Block of Halichondrins and Eribulin. Organic Letters. 14(2). 660–663. 14 indexed citations
9.
Towle, Murray J., Kathleen A. Salvato, Bruce F. Wels, et al.. (2010). Eribulin Induces Irreversible Mitotic Blockade: Implications of Cell-Based Pharmacodynamics for In vivo Efficacy under Intermittent Dosing Conditions. Cancer Research. 71(2). 496–505. 111 indexed citations
10.
Papaioannou, Nikolaos, et al.. (2007). Product‐Regulation Mechanisms for Fatty Acid Biosynthesis Catalyzed by Mycobacterium smegmatis FAS I. ChemBioChem. 8(15). 1775–1780. 10 indexed citations
11.
Minehan, Thomas G. & Yoshito Kishi. (1999). Total Synthesis of the Proposed Structure of (+)-Tolyporphin AO,O-Diacetate. Angewandte Chemie International Edition. 38(7). 923–925. 47 indexed citations
12.
Qiao, Jennifer X. & Yoshito Kishi. (1999). Covalently Cross-Linked Watson-Crick Base Pair Models. Angewandte Chemie International Edition. 38(7). 928–931. 23 indexed citations
13.
Guo, Jiasheng, Kevin J. Duffy, Kirk L. Stevens, et al.. (1998). Total Synthesis of Altohyrtin A (Spongistatin 1): Part 1. Angewandte Chemie International Edition. 37(1-2). 187–190. 105 indexed citations
14.
Shimomura, Osamu, et al.. (1993). Structure and non‐enzymatic light emission of two luciferin precursors isolated from the luminous mushroom Panellus stipticus. Journal of Bioluminescence and Chemiluminescence. 8(4). 201–205. 14 indexed citations
15.
Kong, Fang, Yoshito Kishi, Dolores Pérez‐Sala, & Robert R. Rando. (1990). The stereochemical requirement for protein kinase C activation by 3‐methyldiglycerides matches that found in naturally occurring tumor promoters aplysiatoxins. FEBS Letters. 274(1-2). 203–206. 6 indexed citations
16.
Wang, Yuan, et al.. (1987). Synthesis of C-disaccharides. The Journal of Organic Chemistry. 52(7). 1370–1372. 65 indexed citations
17.
Christ, William J., Jennifer M. Finan, Yoshito Kishi, et al.. (1983). ChemInform Abstract: STEREOCHEMISTRY OF PALYTOXIN. PART 4. COMPLETE STRUCTURE. Chemischer Informationsdienst. 14(12). 18 indexed citations
18.
Christ, William J., et al.. (1982). Stereochemistry of palytoxin. 3. C7-C51 segment. Journal of the American Chemical Society. 104(25). 7367–7369. 3 indexed citations
19.
Goto, Toshio, Yoshito Kishi, Sho Takahashi, & Yoshimasa Hiratå. (1964). The Structures of Tetrodotoxin and Anhydroepitetrodotoxin. Nippon kagaku zassi. 85(10). 661–666,A52. 2 indexed citations
20.
Goto, Toshio & Yoshito Kishi. (1962). The Effect of Metal Salts on the Borohydride Reduction of 5a-Diacet3β, 5α-Diacetoxy-7α-bromocholestan-6-one. Nippon kagaku zassi. 83(10). 1135–1137,A72. 1 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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026