Remo Gandolfi

1.9k total citations
102 papers, 1.5k citations indexed

About

Remo Gandolfi is a scholar working on Organic Chemistry, Physical and Theoretical Chemistry and Pharmaceutical Science. According to data from OpenAlex, Remo Gandolfi has authored 102 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 101 papers in Organic Chemistry, 22 papers in Physical and Theoretical Chemistry and 19 papers in Pharmaceutical Science. Recurrent topics in Remo Gandolfi's work include Organic Chemistry Cycloaddition Reactions (62 papers), Chemical Reaction Mechanisms (22 papers) and Fluorine in Organic Chemistry (19 papers). Remo Gandolfi is often cited by papers focused on Organic Chemistry Cycloaddition Reactions (62 papers), Chemical Reaction Mechanisms (22 papers) and Fluorine in Organic Chemistry (19 papers). Remo Gandolfi collaborates with scholars based in Italy, France and Germany. Remo Gandolfi's co-authors include Armando Rastelli, Mauro Freccero, Carlo De Micheli, Mirko Sarzi-Amadè, Giorgio Bianchi, Paolo Grünanger, Cristiana Di Valentin, Anna Gamba, Lucio Toma and Roberta Oberti and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron.

In The Last Decade

Remo Gandolfi

97 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Remo Gandolfi Italy 22 1.3k 262 181 179 157 102 1.5k
R. W. STROZIER United States 11 965 0.7× 164 0.6× 162 0.9× 152 0.8× 92 0.6× 14 1.1k
Pierluigi Caramella Italy 26 2.0k 1.5× 479 1.8× 236 1.3× 240 1.3× 140 0.9× 85 2.2k
Heinz G. Viehe Belgium 18 1.3k 1.0× 174 0.7× 282 1.6× 95 0.5× 121 0.8× 70 1.5k
Rory A. More O‘Ferrall Ireland 22 1.1k 0.8× 311 1.2× 121 0.7× 163 0.9× 99 0.6× 92 1.4k
Joseph J. Gajewski United States 25 1.5k 1.1× 256 1.0× 145 0.8× 312 1.7× 140 0.9× 96 1.9k
Nguyên Trong Anh France 21 738 0.6× 150 0.6× 78 0.4× 147 0.8× 107 0.7× 39 1.0k
Willi Sicking Germany 21 859 0.6× 314 1.2× 58 0.3× 123 0.7× 103 0.7× 40 1.1k
Engelbert Ciganek United States 25 1.2k 0.9× 167 0.6× 117 0.6× 62 0.3× 97 0.6× 53 1.4k
W. H. DE WOLF Netherlands 22 1.2k 0.9× 309 1.2× 48 0.3× 145 0.8× 219 1.4× 90 1.4k
David M. Birney United States 26 1.6k 1.2× 153 0.6× 69 0.4× 263 1.5× 106 0.7× 56 1.9k

Countries citing papers authored by Remo Gandolfi

Since Specialization
Citations

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

Fields of papers citing papers by Remo Gandolfi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Remo Gandolfi

This figure shows the co-authorship network connecting the top 25 collaborators of Remo Gandolfi. A scholar is included among the top collaborators of Remo Gandolfi 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 Remo Gandolfi. Remo Gandolfi 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.
Annese, Cosimo, Lucia D’Accolti, Caterina Fusco, et al.. (2009). Oxyfunctionalization of Non-Natural Targets by Dioxiranes. 6. On the Selective Hydroxylation of Cubane. Organic Letters. 11(16). 3574–3577. 15 indexed citations
2.
Verga, Daniela, Sara N. Richter, Manlio Palumbo, Remo Gandolfi, & Mauro Freccero. (2006). Bipyridyl ligands as photoactivatable mono- and bis-alkylating agents capable of DNA cross-linking. Organic & Biomolecular Chemistry. 5(2). 233–235. 20 indexed citations
3.
Freccero, Mauro & Remo Gandolfi. (2005). Modeling Acid and Cationic Catalysis on the Reactivity of Duocarmycins. The Journal of Organic Chemistry. 70(18). 7098–7106. 7 indexed citations
4.
Freccero, Mauro, Remo Gandolfi, & Mirko Sarzi-Amadè. (2003). Selectivity of Purine Alkylation by a Quinone Methide. Kinetic or Thermodynamic Control?. The Journal of Organic Chemistry. 68(16). 6411–6423. 35 indexed citations
5.
Valentin, Cristiana Di, Mauro Freccero, Remo Gandolfi, & Armando Rastelli. (2001). ChemInform Abstract: Concerted vs. Stepwise Mechanism in 1,3‐Dipolar Cycloaddition of Nitrone to Ethene, Cyclobutadiene, and Benzocyclobutadiene. A Computational Study.. ChemInform. 32(1). 2 indexed citations
7.
Freccero, Mauro, et al.. (1997). Facial selectivity in the reactions of 1,3-dipoles with cis- and trans-3,4-dimethyl-1-methoxycarbonyl cyclobutenes. Tetrahedron. 53(27). 9279–9292. 3 indexed citations
9.
10.
Gandolfi, Remo, et al.. (1993). 2,3-Dioxabicyclo[2.2.2]oct-5-ene: a pyramidalized olefin whose facial selectivity does not parallel its pyramidalization. The Journal of Organic Chemistry. 58(22). 6038–6048. 26 indexed citations
11.
Rastelli, Armando, et al.. (1990). syn–anti Isomerism in the 1,3‐dipolar cycloaddition to cis‐3,4‐disubstituted cyclobutenes. 4. Intramolecular interactions. Journal of Physical Organic Chemistry. 3(3). 159–173. 11 indexed citations
12.
Gandolfi, Remo, et al.. (1988). Syn-anti isomerism in the 1,3-dipolar cycloaddition to cis-3,4-disubstituted cyclobutenes. 3. Charge-transfer electrostatic, and steric effects. The Journal of Organic Chemistry. 53(9). 2123–2125. 10 indexed citations
13.
Benedetti, Pier G. De, Carlo De Micheli, Remo Gandolfi, Pierluigi Gariboldi, & Armando Rastelli. (1980). 1,3-Dipolar cycloadditions of diazoalkanes with thiete 1,1-dioxide. The Journal of Organic Chemistry. 45(18). 3646–3650. 9 indexed citations
14.
Gandolfi, Remo, Lucio Toma, & Carlo De Micheli. (1979). 1,3-Dipolar Cycloreversions of Isoxazolidines and Pyrazolidines. Heterocycles. 12(1). 5–5. 4 indexed citations
15.
Bianchi, Giorgio, et al.. (1977). Δ2-Isoxazoline derivatives. Part 11. Reactions of nitrile oxides, diazoalkanes, and dienes with 2-oxa-3-azabicyclo[3.2.0]hepta-3,6-diene derivatives. Journal of the Chemical Society Perkin Transactions 1. 2222–2227. 2 indexed citations
16.
17.
Bianchi, Giorgio, et al.. (1973). Isoxazoline derivatives. Part VI. Regioselectivity in the 1,3-dipolar cycloaddition of nitrile oxides to αβ-unsaturated ketones. Journal of the Chemical Society Perkin Transactions 1. 1148–1155. 52 indexed citations
18.
Bianchi, Giorgio, Remo Gandolfi, & Paolo Grünanger. (1973). Cycoladdition of nitrile imines to cyclooctatetraene. Tetrahedron. 29(16). 2405–2410. 7 indexed citations
19.
Bianchi, Giacomo, Remo Gandolfi, & Paolo Grünanger. (1970). 2-Isoxazoline derivatives—III. Tetrahedron. 26(21). 5113–5122. 14 indexed citations
20.
Bianchi, Giorgio, Remo Gandolfi, & Paolo Grünanger. (1968). 2‐Isoxazoline derivatives. Part I. A base‐promoted fragmentation of 2‐isoxazolines. Journal of Heterocyclic Chemistry. 5(1). 49–52. 20 indexed citations

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