José E. D. Martins

678 total citations
18 papers, 606 citations indexed

About

José E. D. Martins is a scholar working on Inorganic Chemistry, Organic Chemistry and Biomedical Engineering. According to data from OpenAlex, José E. D. Martins has authored 18 papers receiving a total of 606 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Inorganic Chemistry, 8 papers in Organic Chemistry and 8 papers in Biomedical Engineering. Recurrent topics in José E. D. Martins's work include Asymmetric Hydrogenation and Catalysis (12 papers), Catalysis for Biomass Conversion (8 papers) and Asymmetric Synthesis and Catalysis (6 papers). José E. D. Martins is often cited by papers focused on Asymmetric Hydrogenation and Catalysis (12 papers), Catalysis for Biomass Conversion (8 papers) and Asymmetric Synthesis and Catalysis (6 papers). José E. D. Martins collaborates with scholars based in United Kingdom and Brazil. José E. D. Martins's co-authors include Martin Wills, Guy J. Clarkson, Daljit S. Matharu, David J. Morris, Valentim Emı́lio Uberti Costa, Jamie Godfrey, Tarn C. Johnson, Fung Kei Cheung, Rina Soni and M. A. Graham and has published in prestigious journals such as Tetrahedron, Organic Letters and Tetrahedron Letters.

In The Last Decade

José E. D. Martins

16 papers receiving 601 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
José E. D. Martins United Kingdom	12	506	346	244	170	135	18	606
Ziyuan Ding China	10	759 1.5×	647 1.9×	374 1.5×	212 1.2×	86 0.6×	13	908
Mario P. Wiesenfeldt Germany	10	481 1.0×	679 2.0×	156 0.6×	90 0.5×	93 0.7×	16	846
Manabu Kashiwabara Japan	6	415 0.8×	431 1.2×	203 0.8×	115 0.7×	46 0.3×	9	587
Martin A. Ariger Switzerland	8	751 1.5×	960 2.8×	107 0.4×	233 1.4×	73 0.5×	9	1.1k
Neil T. Fairweather United States	7	311 0.6×	277 0.8×	122 0.5×	118 0.7×	140 1.0×	9	503
Bernhard Beiring Germany	9	427 0.8×	742 2.1×	135 0.6×	63 0.4×	64 0.5×	9	841
Long‐Sheng Zheng China	17	363 0.7×	475 1.4×	134 0.5×	158 0.9×	81 0.6×	25	652
Naim Menashe Israel	6	250 0.5×	266 0.8×	71 0.3×	81 0.5×	81 0.6×	8	378
Kathelyne Everaere France	8	632 1.2×	362 1.0×	321 1.3×	228 1.3×	181 1.3×	9	728
Fenja R. Schoepke Germany	5	457 0.9×	655 1.9×	90 0.4×	231 1.4×	28 0.2×	6	745

Countries citing papers authored by José E. D. Martins

Since Specialization

Citations

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

Fields of papers citing papers by José E. D. Martins

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by José E. D. Martins. 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 José E. D. Martins. The network helps show where José E. D. Martins may publish in the future.

Co-authorship network of co-authors of José E. D. Martins

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

All Works

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18 of 18 papers shown

Martins, José E. D., et al.. (2024). Inclusão e acessibilidade digital no ambiente escolar. Contribuciones a las Ciencias Sociales. 17(10). e11675–e11675.

Martins, José E. D., et al.. (2011). Developing asymmetric iron and ruthenium-based cyclone complexes; complex factors influence the asymmetric induction in the transfer hydrogenation of ketones. Organic & Biomolecular Chemistry. 10(1). 134–145. 71 indexed citations

Soni, Rina, et al.. (2011). The importance of the N–H bond in Ru/TsDPEN complexes for asymmetric transfer hydrogenation of ketones and imines. Organic & Biomolecular Chemistry. 9(9). 3290–3290. 76 indexed citations

Martins, José E. D., et al.. (2010). Applications of N′-alkylated derivatives of TsDPEN in the asymmetric transfer hydrogenation of C O and C N bonds. Tetrahedron Asymmetry. 21(18). 2258–2264. 45 indexed citations

Martins, José E. D., Guy J. Clarkson, & Martin Wills. (2009). Ru(II) Complexes of N-Alkylated TsDPEN Ligands in Asymmetric Transfer Hydrogenation of Ketones and Imines. Organic Letters. 11(4). 847–850. 145 indexed citations

Martins, José E. D. & Martin Wills. (2009). Ir(III) complexes of diamine ligands for asymmetric ketone hydrogenation. Tetrahedron. 65(29-30). 5782–5786. 35 indexed citations

Matharu, Daljit S., José E. D. Martins, & Martin Wills. (2008). Asymmetric Transfer Hydrogenation of CO and CN Bonds by Tethered Rh^III Catalysts. Chemistry - An Asian Journal. 3(8-9). 1374–1383. 73 indexed citations

Martins, José E. D. & Martin Wills. (2008). Synthesis of a series of novel N,N-dialkyl-TsDPEN ligands and their application to enantioselective addition of dialkylzinc to benzaldehyde. Tetrahedron Asymmetry. 19(10). 1250–1255. 28 indexed citations

Martins, José E. D., et al.. (2008). Further ‘tethered’ Ru(II) catalysts for asymmetric transfer hydrogenation (ATH) of ketones; the use of a benzylic linker and a cyclohexyldiamine ligand. Journal of Organometallic Chemistry. 693(23). 3527–3532. 38 indexed citations

10.

Martins, José E. D., David J. Morris, & Martin Wills. (2008). Asymmetric hydrogenation of ketones using Ir(III) complexes of N-alkyl-N’-tosyl-1,2-ethanediamine ligands. Tetrahedron Letters. 50(6). 688–692. 35 indexed citations

11.

Martins, José E. D., et al.. (2006). Synthesis of chiral norbornane derivatives as γ-amino alcohol catalysts: the effect of the functional group positions on the chirality transfer. Tetrahedron Asymmetry. 17(12). 1817–1823. 13 indexed citations

12.

Martins, José E. D.. (2006). Ammonia: A Versatile Reagent in Organic Chemistry. Synlett. 2006(6). 962–963. 2 indexed citations

13.

Martins, José E. D., Luciane F. de Oliveira, & Valentim Emı́lio Uberti Costa. (2006). New Efficient Route to the Synthesis of Enantiopure (+) and (−) Bicyclo[2.2.1]heptan‐syn‐2,7‐diol using Lipase‐Catalyzed Transesterifications. Synthetic Communications. 36(22). 3419–3424.

14.

Lapis, Alexandre A.M., Ângelo de Fátima, José E. D. Martins, Valentim Emı́lio Uberti Costa, & Ronaldo A. Pilli. (2005). Asymmetric Reduction of Prochiral Ketones Using in situ Generated Oxazaborolidine Derived from (1S,2S,3R,4R)‐3‐Amino‐7,7‐dimethoxynorbornan‐2‐ol. An Efficient Synthesis of Enantiopure (R)‐Tomoxetine.. ChemInform. 36(19). 1 indexed citations

15.

Lapis, Alexandre A.M., Ângelo de Fátima, José E. D. Martins, Valentim Emı́lio Uberti Costa, & Ronaldo A. Pilli. (2004). Asymmetric reduction of prochiral ketones using in situ generated oxazaborolidine derived from (1S,2S,3R,4R)-3-amino-7,7-dimethoxynorbornan-2-ol. An efficient synthesis of enantiopure (R)-tomoxetine. Tetrahedron Letters. 46(3). 495–498. 20 indexed citations

16.

Martins, José E. D., et al.. (2003). Study of the kinetic resolution of (±)-10-exo-hydroxy-pentacyclo[6.2.1.13,6.02,7.05,9]dodeca-4-one by lipase catalysis and the intramolecular racemization of the pure enantiomer by thermal dyotropic reaction. Tetrahedron Asymmetry. 14(6). 683–688. 3 indexed citations

17.

Lapis, Alexandre A.M., et al.. (2001). On the mechanism of skeletal rearrangements in the acid catalysed acetylation of isodrin †. Journal of the Chemical Society Perkin Transactions 2. 7–12. 5 indexed citations

18.

Costa, Valentim Emı́lio Uberti, et al.. (1998). Evaluation of lipase from Candida rugosa in the resolution of endo-(±)-1,8,9,10,11,11-hexachloropentacyclo[6.2.1.13,6.02,7.05,9]dodecan-4-alcohol. Tetrahedron Asymmetry. 9(15). 2579–2585. 16 indexed citations

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