J. M. SAA

2.8k total citations
116 papers, 2.2k citations indexed

About

J. M. SAA is a scholar working on Organic Chemistry, Biochemistry and Molecular Biology. According to data from OpenAlex, J. M. SAA has authored 116 papers receiving a total of 2.2k indexed citations (citations by other indexed papers that have themselves been cited), including 94 papers in Organic Chemistry, 20 papers in Biochemistry and 17 papers in Molecular Biology. Recurrent topics in J. M. SAA's work include Asymmetric Synthesis and Catalysis (31 papers), Traditional and Medicinal Uses of Annonaceae (19 papers) and Asymmetric Hydrogenation and Catalysis (12 papers). J. M. SAA is often cited by papers focused on Asymmetric Synthesis and Catalysis (31 papers), Traditional and Medicinal Uses of Annonaceae (19 papers) and Asymmetric Hydrogenation and Catalysis (12 papers). J. M. SAA collaborates with scholars based in Spain, United States and Italy. J. M. SAA's co-authors include Carmén Nájera, José M. Sansano, Gabriel Martorell, Jesús Casas, Luís Castedo, Alejandro Baeza, Fernando Tur, Rafael Suau, A. García‐Raso and Pere M. Deyà and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemical Communications.

In The Last Decade

J. M. SAA

116 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
J. M. SAA Spain 27 1.8k 434 425 206 161 116 2.2k
Kiyoharu Nishide Japan 27 1.7k 0.9× 572 1.3× 304 0.7× 111 0.5× 167 1.0× 103 2.1k
Tse‐Lok Ho Canada 23 1.8k 1.0× 512 1.2× 309 0.7× 103 0.5× 134 0.8× 172 2.1k
Kunihiko Takabe Japan 26 2.3k 1.3× 1.0k 2.3× 399 0.9× 218 1.1× 183 1.1× 145 2.7k
Arrigo Scettri Italy 30 2.8k 1.5× 504 1.2× 580 1.4× 168 0.8× 176 1.1× 161 3.2k
Takefumi Momose Japan 25 1.9k 1.0× 548 1.3× 183 0.4× 138 0.7× 145 0.9× 186 2.2k
Hiroshi Suginome Japan 27 2.5k 1.4× 595 1.4× 303 0.7× 111 0.5× 97 0.6× 228 3.0k
Yoo Tanabe Japan 32 2.5k 1.4× 740 1.7× 282 0.7× 113 0.5× 167 1.0× 140 2.9k
Yong Qiang Tu China 26 2.4k 1.3× 506 1.2× 617 1.5× 130 0.6× 71 0.4× 66 2.9k
R. H. Schlessinger United States 29 2.1k 1.2× 558 1.3× 152 0.4× 190 0.9× 181 1.1× 123 2.5k
Arthur G. Schultz United States 28 2.4k 1.3× 549 1.3× 239 0.6× 165 0.8× 126 0.8× 178 2.8k

Countries citing papers authored by J. M. SAA

Since Specialization
Citations

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

Fields of papers citing papers by J. M. SAA

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of J. M. SAA

This figure shows the co-authorship network connecting the top 25 collaborators of J. M. SAA. A scholar is included among the top collaborators of J. M. SAA 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 J. M. SAA. J. M. SAA 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.
Bari, Lorenzo Di, et al.. (2010). [Ln(binolam)3]⋅(OTf)3, a New Class of Propeller‐Shaped Lanthanide(III) Salt Complexes as Enantioselective Catalysts: Structure, Dynamics and Mechanistic Insight. Chemistry - A European Journal. 16(47). 14190–14201. 19 indexed citations
2.
SAA, J. M. & Manuel Yáñez. (2009). On the “Gluing” Effect of Lithium: The Lithium‐Driven Assembly of Circum‐Arranged, Edge‐Fused Cyclopentadienyl Lithium Compounds and Aza Analogues. Chemistry - A European Journal. 15(13). 3123–3129. 4 indexed citations
4.
Baeza, Alejandro, Carmén Nájera, José M. Sansano, & J. M. SAA. (2005). Binolam–AlCl: A Two‐Centre Catalyst for the Synthesis of Enantioenriched Cyanohydrin O‐Phosphates. Chemistry - A European Journal. 11(13). 3849–3862. 50 indexed citations
5.
Baeza, Alejandro, Jesús Casas, Carmén Nájera, José M. Sansano, & J. M. SAA. (2003). Enantioselective Synthesis of Cyanohydrin O‐Phosphates Mediated by the Bifunctional Catalyst Binolam–AlCl. Angewandte Chemie International Edition. 42(27). 3143–3146. 76 indexed citations
6.
Casas, Jesús, Alejandro Baeza, José M. Sansano, Carmén Nájera, & J. M. SAA. (2003). Enantioselective cyanoformylation of aldehydes mediated by BINOLAM–AlCl as a monometallic bifunctional catalyst. Tetrahedron Asymmetry. 14(2). 197–200. 79 indexed citations
7.
SAA, J. M., et al.. (2002). Self-assembly of a stereoselective trinuclear sodium/lithium triple helix. Chemical Communications. 1982–1983. 14 indexed citations
8.
Casas, Jesús, et al.. (2001). Enantioselective synthesis of (S)-α-methylphenylalanine using (S)-BINOLAMs as new phase-transfer catalysts. Tetrahedron Asymmetry. 12(5). 699–702. 33 indexed citations
10.
Martorell, Gabriel, A. García‐Raso, & J. M. SAA. (1990). Palladium catalyzed cross-coupling of phenol triflates with organostannanes. A versatile approach for the synthesis of substituted resorcinol dimethyl ethers.. Tetrahedron Letters. 31(16). 2357–2360. 25 indexed citations
11.
Morey, Jeroni, et al.. (1990). Direct lithiation of alkoxyphenols: metalation versus demethylation. An experimental and theoretical (MNDO) study. The Journal of Organic Chemistry. 55(12). 3902–3909. 15 indexed citations
12.
Guitián, Enrique, et al.. (1987). Novel entry into the benzo(C)phenanthridine skeleton through the intermolecular benzyne cycloaddition (IBC) approach. Tetrahedron Letters. 28(21). 2407–2408. 7 indexed citations
13.
Guitián, Enrique, et al.. (1987). The reaction of 1-alkyldihydroisoquinolines with benzyne. An unexpected entry to dibenzindolizines.. Tetrahedron Letters. 28(7). 817–820. 11 indexed citations
15.
SAA, J. M., et al.. (1986). A novel degradative strategy for the synthesis of p-quinones.. Tetrahedron Letters. 27(42). 5125–5128. 10 indexed citations
16.
Castedo, Luís, Domingo Domı́nguez, Ángel R. de Lera, et al.. (1984). New oxidized isocularine alkaloids from sarcocapnos plants. Tetrahedron Letters. 25(51). 5933–5936. 23 indexed citations
17.
Castedo, Luís, et al.. (1983). Ribasidine, a new ribasine alkaloid. Structure and characterization. Tetrahedron Letters. 24(41). 4481–4484. 13 indexed citations
18.
SAA, J. M. & Michael P. Cava. (1978). ChemInform Abstract: DEHYDROAPORPHINES. AN ACYLATION STUDY. Chemischer Informationsdienst. 9(38). 9 indexed citations
19.
Castedo, Luís, Domingo Domı́nguez, J. M. SAA, & Rafael Suau. (1978). Luguine, a new benzophenanthridine alkaloid from glaucium flavum cr. var. vestitum. Tetrahedron Letters. 19(32). 2923–2924. 5 indexed citations
20.
SAA, J. M., M. V. Lakshmikantham, Michael J. Mitchell, & Michael P. Cava. (1976). Krukovine, a new bis(benzylisoquinoline) alkaloid from Abuta splendida. The Journal of Organic Chemistry. 41(2). 317–319. 10 indexed citations

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