Martin J. Lear

1.9k total citations
72 papers, 1.6k citations indexed

About

Martin J. Lear is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Martin J. Lear has authored 72 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Organic Chemistry, 27 papers in Molecular Biology and 18 papers in Pharmacology. Recurrent topics in Martin J. Lear's work include Microbial Natural Products and Biosynthesis (15 papers), Synthetic Organic Chemistry Methods (15 papers) and Chemical Synthesis and Analysis (12 papers). Martin J. Lear is often cited by papers focused on Microbial Natural Products and Biosynthesis (15 papers), Synthetic Organic Chemistry Methods (15 papers) and Chemical Synthesis and Analysis (12 papers). Martin J. Lear collaborates with scholars based in Japan, Singapore and United Kingdom. Martin J. Lear's co-authors include Masahiro Hirama, Yujiro Hayashi, Fumihiko Yoshimura, Mun Hong Ngai, Markus R. Wenk, Jing Li, Kai Liu, Pengyu Yang, Shao Q. Yao and Stanley T.‐C. Eey and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Nature Communications.

In The Last Decade

Martin J. Lear

72 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Martin J. Lear Japan	23	1.0k	593	203	179	109	72	1.6k
Guillermo R. Labadié Argentina	20	594 0.6×	483 0.8×	107 0.5×	123 0.7×	95 0.9×	73	1.2k
Gerd K. Wagner United Kingdom	26	961 0.9×	1.1k 1.8×	92 0.5×	63 0.4×	145 1.3×	82	1.9k
Roman Manetsch United States	23	1.4k 1.4×	1.0k 1.7×	184 0.9×	260 1.5×	59 0.5×	64	2.0k
Paulo R. R. Costa Brazil	26	1.3k 1.2×	760 1.3×	254 1.3×	230 1.3×	95 0.9×	185	2.4k
Maria M. M. Santos Portugal	27	1.3k 1.3×	731 1.2×	94 0.5×	113 0.6×	370 3.4×	71	2.1k
Suely Lins Galdino Brazil	22	606 0.6×	513 0.9×	127 0.6×	136 0.8×	90 0.8×	84	1.5k
Siegfried S. F. Leung United States	14	513 0.5×	921 1.6×	119 0.6×	98 0.5×	142 1.3×	14	1.4k
Sivaraman Dandapani United States	19	914 0.9×	928 1.6×	121 0.6×	44 0.2×	101 0.9×	54	1.7k
Giuseppe La Regina Italy	33	2.1k 2.0×	945 1.6×	265 1.3×	59 0.3×	217 2.0×	105	3.4k
Rebecca Deprez‐Poulain France	24	941 0.9×	733 1.2×	117 0.6×	164 0.9×	220 2.0×	61	1.7k

Countries citing papers authored by Martin J. Lear

Since Specialization

Citations

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

Fields of papers citing papers by Martin J. Lear

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Martin J. Lear

This figure shows the co-authorship network connecting the top 25 collaborators of Martin J. Lear. A scholar is included among the top collaborators of Martin J. Lear 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 Martin J. Lear. Martin J. Lear 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

Wang, Xiaonan, et al.. (2025). Chemoselective synthesis of 1,3,4-thiadiazoles from acyl hydrazines and nitroalkanes using elemental sulfur. Nature Communications. 16(1). 6127–6127. 1 indexed citations

Li, Yuanhang, Shaohong Wang, Silong Xu, et al.. (2025). Light‐Dependent Amide or Thioamide Formation of Acylsilanes with Amines using Elemental Sulfur. Chemistry - A European Journal. 31(12). e202404555–e202404555. 2 indexed citations

Kobayashi, Shōji, et al.. (2023). One‐Pot Conversion of Benzyl Alcohols to N‐Protected Anilines and Alkyl Alcohols to Carbamoyl Azides. European Journal of Organic Chemistry. 26(47). 1 indexed citations

Wang, Xiaonan, Silong Xu, Yuhai Tang, et al.. (2023). Nitroalkanes as thioacyl equivalents to access thioamides and thiopeptides. Nature Communications. 14(1). 4626–4626. 25 indexed citations

Sekar, Karthik, et al.. (2021). Cis Selective RCM Study to the 14-Membered Cyclic Subunit of Bielschowskysin. The Journal of Organic Chemistry. 86(9). 6160–6168. 1 indexed citations

Li, Jing, Eunsang Kwon, Martin J. Lear, & Yujiro Hayashi. (2021). Halogen Bonding of N‐Halosuccinimides with Amines and Effects of Brønsted Acids in Quinuclidine‐Catalyzed Halocyclizations. Helvetica Chimica Acta. 104(9). 16 indexed citations

Lear, Martin J., et al.. (2019). A convergent total synthesis of the kedarcidin chromophore: 20-years in the making. The Journal of Antibiotics. 72(6). 350–363. 11 indexed citations

Ochs, Christopher J., Aïcha Boudhar, Gomathy Sandhya Subramanian, et al.. (2014). Design, preparation and assessment of surface-immobilised tetraphenylethenes for biosensing applications. Applied Surface Science. 307. 475–481. 3 indexed citations

Suwanarusk, Rossarin, Yan Quan Lee, Kitti Wing Ki Chan, et al.. (2014). Characterization of the Commercially-Available Fluorescent Chloroquine-BODIPY Conjugate, LynxTag-CQGREEN, as a Marker for Chloroquine Resistance and Uptake in a 96-Well Plate Assay. PLoS ONE. 9(10). e110800–e110800. 4 indexed citations

10.

Yamada, Kei, Martin J. Lear, Shuji Yamashita, et al.. (2014). Biomimetic Total Synthesis of Cyanosporaside Aglycons from a Single Enediyne Precursor through Site‐Selective p‐Benzyne Hydrochlorination. Angewandte Chemie International Edition. 53(50). 13902–13906. 34 indexed citations

11.

Glover, Robert P., Yicun Huang, Horst Flotow, et al.. (2013). Isolation and synthesis of falcitidin, a novel myxobacterial-derived acyltetrapeptide with activity against the malaria target falcipain-2. The Journal of Antibiotics. 66(5). 259–264. 12 indexed citations

12.

Lam, Sin Man, et al.. (2013). Rapid and sensitive profiling of tear wax ester species using high performance liquid chromatography coupled with tandem mass spectrometry. Journal of Chromatography A. 1308. 166–171. 26 indexed citations

13.

Gorelik, Sergey, et al.. (2013). Transient absorption spectroscopy on spiropyran monolayers using nanosecond pump—probe Brewster angle reflectometry. Photochemical & Photobiological Sciences. 12(5). 848–853. 3 indexed citations

14.

Gorelik, Sergey, Anton Sadovoy, Martin J. Lear, et al.. (2012). Photoconversion of Spiropyran to Merocyanine in a Monolayer Observed Using Nanosecond Pump-Probe Brewster Angle Reflectometry. Australian Journal of Chemistry. 65(3). 283–289. 3 indexed citations

15.

Yang, Pengyu, Min Wang, Kai Liu, et al.. (2012). Parasite‐Based Screening and Proteome Profiling Reveal Orlistat, an FDA‐Approved Drug, as a Potential Anti Trypanosoma brucei Agent^[^]. Chemistry - A European Journal. 18(27). 8403–8413. 14 indexed citations

16.

Gorelik, Sergey, et al.. (2009). Transient Brewster angle reflectometry of spiropyran monolayers. Photochemical & Photobiological Sciences. 9(2). 141–151. 6 indexed citations

17.

Song, Hong, et al.. (2009). Practical synthesis of maleimides and coumarin-linked probes for protein and antibody labelling via reduction of native disulfides. Organic & Biomolecular Chemistry. 7(17). 3400–3400. 79 indexed citations

18.

Usuki, Toyonobu, Martin J. Lear, Parthasarathi Das, et al.. (2004). Spin Trapping of ¹³C‐Labeled p‐Benzynes Generated by Masamune–Bergman Cyclization of Bicyclic Nine‐Membered Enediynes. Angewandte Chemie International Edition. 43(39). 5249–5253. 29 indexed citations

19.

Lear, Martin J., Fumihiko Yoshimura, & Masahiro Hirama. (2001). A Direct and Efficientα-Selective Glycosylation Protocol for the Kedarcidin Sugar,L-Mycarose: AgPF6 as a Remarkable Activator of 2-Deoxythioglycosides. Angewandte Chemie International Edition. 40(5). 946–949. 54 indexed citations

20.

McLeod, HL, et al.. (1996). In vivo pharmacology and anti-tumour evaluation of the tyrphostin tyrosine kinase inhibitor RG13022. British Journal of Cancer. 74(11). 1714–1718. 18 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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