Misato Yonemoto

517 total citations
8 papers, 440 citations indexed

About

Misato Yonemoto is a scholar working on Organic Chemistry, Process Chemistry and Technology and Inorganic Chemistry. According to data from OpenAlex, Misato Yonemoto has authored 8 papers receiving a total of 440 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Organic Chemistry, 2 papers in Process Chemistry and Technology and 2 papers in Inorganic Chemistry. Recurrent topics in Misato Yonemoto's work include Asymmetric Synthesis and Catalysis (5 papers), Catalytic Cross-Coupling Reactions (4 papers) and Catalytic C–H Functionalization Methods (3 papers). Misato Yonemoto is often cited by papers focused on Asymmetric Synthesis and Catalysis (5 papers), Catalytic Cross-Coupling Reactions (4 papers) and Catalytic C–H Functionalization Methods (3 papers). Misato Yonemoto collaborates with scholars based in Japan and United Kingdom. Misato Yonemoto's co-authors include Yoshinori Kondo, Kiyofumi Inamoto, Koji Kobayashi, Shoko Kikkawa, Yuka Nakamura, Yoshiyuki Tanaka, Masahiro Hashimoto, Andrew E. H. Wheatley, Hiroshi Naka and Masahiro Ueno and has published in prestigious journals such as Chemical Communications, Organic Letters and Organic & Biomolecular Chemistry.

In The Last Decade

Misato Yonemoto

8 papers receiving 438 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Misato Yonemoto Japan	8	347	126	109	80	45	8	440
Beiqi Sun China	8	268 0.8×	143 1.1×	63 0.6×	115 1.4×	34 0.8×	10	379
Megumi Okada Japan	8	323 0.9×	123 1.0×	119 1.1×	61 0.8×	23 0.5×	9	405
Rosie J. Somerville Spain	11	525 1.5×	81 0.6×	169 1.6×	84 1.1×	45 1.0×	17	628
Joaquim Caner Japan	11	222 0.6×	132 1.0×	136 1.2×	118 1.5×	36 0.8×	16	343
Junting Hong China	8	239 0.7×	152 1.2×	63 0.6×	128 1.6×	27 0.6×	9	354
Yiling Zhu United States	7	264 0.8×	170 1.3×	207 1.9×	102 1.3×	35 0.8×	11	431
Janakiram Vaitla India	17	865 2.5×	133 1.1×	148 1.4×	80 1.0×	23 0.5×	37	963
Wenxuan Xue China	9	274 0.8×	48 0.4×	102 0.9×	34 0.4×	52 1.2×	15	333
Raj Kumar Tak India	13	291 0.8×	108 0.9×	157 1.4×	42 0.5×	19 0.4×	27	419
Prashant Gautam India	8	525 1.5×	161 1.3×	162 1.5×	32 0.4×	19 0.4×	8	596

Countries citing papers authored by Misato Yonemoto

Since Specialization

Citations

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

Fields of papers citing papers by Misato Yonemoto

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Misato Yonemoto

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

All Works

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8 of 8 papers shown

1.

Inamoto, Kiyofumi, et al.. (2013). Organocatalytic functionalization of heteroaromatic N-oxides with C-nucleophiles using in situ generated onium amide bases. Organic & Biomolecular Chemistry. 11(27). 4438–4438. 47 indexed citations

2.

Inamoto, Kiyofumi, et al.. (2012). Organocatalytic deprotonative functionalization of C(sp2)–H and C(sp3)–H bonds using in situ generated onium amide bases. Chemical Communications. 48(78). 9771–9771. 31 indexed citations

3.

Inamoto, Kiyofumi, et al.. (2012). Synthesis of 3-Carboxylated Indoles through a Tandem Process Involving Cyclization of 2-Ethynylanilines Followed by CO₂ Fixation in the Absence of Transition Metal Catalysts. Organic Letters. 14(10). 2622–2625. 58 indexed citations

4.

Inamoto, Kiyofumi, et al.. (2011). Micellar system in copper-catalysed hydroxylation of arylboronic acids: facile access to phenols. Chemical Communications. 47(42). 11775–11775. 115 indexed citations

5.

Inamoto, Kiyofumi, et al.. (2011). A copper-based catalytic system for carboxylation of terminal alkynes: synthesis of alkyl 2-alkynoates. Organic & Biomolecular Chemistry. 10(8). 1514–1514. 81 indexed citations

6.

Kobayashi, Koji, et al.. (2010). Functionalisation of heteroaromatic N-oxides using organic superbase catalyst. Organic & Biomolecular Chemistry. 9(1). 78–80. 40 indexed citations

7.

Kobayashi, Koji, et al.. (2010). Metal-free deprotonative functionalization of heteroaromatics using organic superbase catalyst. Chemical Communications. 46(40). 7623–7623. 24 indexed citations

8.

Ueno, Masahiro, Misato Yonemoto, Masahiro Hashimoto, et al.. (2007). Nucleophilic aromatic substitution using Et3SiH/cat. t-Bu-P4 as a system for nucleophile activation. Chemical Communications. 2264–2264. 44 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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