Maria Bucciarelli

424 total citations
26 papers, 313 citations indexed

About

Maria Bucciarelli is a scholar working on Organic Chemistry, Molecular Biology and Spectroscopy. According to data from OpenAlex, Maria Bucciarelli has authored 26 papers receiving a total of 313 indexed citations (citations by other indexed papers that have themselves been cited), including 20 papers in Organic Chemistry, 9 papers in Molecular Biology and 4 papers in Spectroscopy. Recurrent topics in Maria Bucciarelli's work include Synthesis and Catalytic Reactions (14 papers), Organic Chemistry Cycloaddition Reactions (8 papers) and Enzyme Catalysis and Immobilization (7 papers). Maria Bucciarelli is often cited by papers focused on Synthesis and Catalytic Reactions (14 papers), Organic Chemistry Cycloaddition Reactions (8 papers) and Enzyme Catalysis and Immobilization (7 papers). Maria Bucciarelli collaborates with scholars based in Italy. Maria Bucciarelli's co-authors include Arrigo Forni, Irene Moretti, Giovanni Torre, Fabio Prati, Emilia Caselli, Paolo Davoli, Luciano Antolini, Sergio Brückner, G. D. Andreetti and Remir G. Kostyanovsky and has published in prestigious journals such as The Journal of Organic Chemistry, Tetrahedron and Synthesis.

In The Last Decade

Maria Bucciarelli

26 papers receiving 297 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Maria Bucciarelli Italy 11 225 146 61 36 34 26 313
G. ROUSSEAU France 13 324 1.4× 109 0.7× 59 1.0× 26 0.7× 41 1.2× 26 411
D. G. KULKARNI India 8 226 1.0× 68 0.5× 44 0.7× 18 0.5× 49 1.4× 9 281
Keith E. McCarthy United States 11 341 1.5× 137 0.9× 18 0.3× 32 0.9× 40 1.2× 19 401
Russell C. Klix United States 12 275 1.2× 85 0.6× 25 0.4× 19 0.5× 28 0.8× 16 327
Michael S. Ashwood United Kingdom 12 315 1.4× 157 1.1× 24 0.4× 54 1.5× 54 1.6× 18 377
R. Hui United States 8 216 1.0× 139 1.0× 69 1.1× 10 0.3× 15 0.4× 10 318
Elisa I. León Spain 14 390 1.7× 103 0.7× 23 0.4× 61 1.7× 26 0.8× 34 433
K. M. RYAN United States 6 274 1.2× 104 0.7× 30 0.5× 10 0.3× 59 1.7× 9 313
J. Ian Grayson Switzerland 10 340 1.5× 64 0.4× 33 0.5× 35 1.0× 46 1.4× 18 380
K. AKUTAGAWA United States 14 408 1.8× 101 0.7× 21 0.3× 38 1.1× 58 1.7× 29 455

Countries citing papers authored by Maria Bucciarelli

Since Specialization
Citations

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

Fields of papers citing papers by Maria Bucciarelli

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Bucciarelli

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Bucciarelli. A scholar is included among the top collaborators of Maria Bucciarelli 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 Maria Bucciarelli. Maria Bucciarelli 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.
Davoli, Paolo, et al.. (2008). ChemInform Abstract: A Mild Synthesis of Nitriles by TPPX2‐Promoted Dehydration of Primary Amides.. ChemInform. 39(3). 1 indexed citations
2.
Caselli, Emilia, et al.. (2005). Enantiomeric excess of 1,2-diols by formation of cyclic boronates: an improved method. Tetrahedron Asymmetry. 16(17). 2918–2926. 22 indexed citations
3.
Caselli, Emilia, Giovanni Tosi, Arrigo Forni, Maria Bucciarelli, & Fabio Prati. (2003). Chemo-enzymatic synthesis of levodropropizine. Il Farmaco. 58(10). 1029–1032. 3 indexed citations
4.
Davoli, Paolo, Emilia Caselli, Maria Bucciarelli, et al.. (2002). Lipase-catalyzed resolution and desymmetrization of 2-hydroxymethylaziridines. Journal of the Chemical Society Perkin Transactions 1. 1948–1953. 7 indexed citations
5.
Forni, Arrigo, Emilia Caselli, Fabio Prati, Maria Bucciarelli, & Giovanni Torre. (2002). Highly enantioselective reduction of ethyl 4-chloro-3-oxobutanoate to L- and D- 3-hydroxyesters with baker’s yeast. ARKIVOC. 2002(11). 45–53. 5 indexed citations
6.
Antolini, Luciano, Maria Bucciarelli, Emilia Caselli, et al.. (1997). Stereoselective Synthesis of Erythro β-Substituted Aspartates. The Journal of Organic Chemistry. 62(25). 8784–8789. 30 indexed citations
7.
Bucciarelli, Maria, Arrigo Forni, Irene Moretti, Fabio Prati, & Giovanni Torre. (1995). Regioselectivity of ring-opening reactions of optically active N-acetyl-2-methoxycarbonylaziridine. Tetrahedron Asymmetry. 6(8). 2073–2080. 26 indexed citations
8.
Antolini, Luciano, Maria Bucciarelli, Arrigo Forni, et al.. (1992). Optically active cis- and trans-1-chloro-2-methoxycarbonyl-2-methylcarbamoylaziridines. Stereochemical properties. Journal of the Chemical Society Perkin Transactions 2. 959–959. 3 indexed citations
9.
Antolini, Luciano, Maria Bucciarelli, Arrigo Forni, Irene Moretti, & Fabio Prati. (1991). Derivatives of optically active 1-chloro-2,2-bismethoxycarbonylaziridine: absolute configuration and X-ray molecular structure of (–)-(E)-1-chloro-2-methoxycarbonyl-2-methylcarbamoylaziridine. Journal of the Chemical Society Chemical Communications. 538–539. 10 indexed citations
10.
Bucciarelli, Maria, Arrigo Forni, Irene Moretti, & Fabio Prati. (1990). Optically active N-chloro-2,2-bismethoxycarbonylaziridine by enzymatic hydrolysis.. Tetrahedron Asymmetry. 1(1). 5–8. 10 indexed citations
11.
12.
Bucciarelli, Maria, Arrigo Forni, Irene Moretti, & Giovanni Torre. (1983). Influence of the N-sulphonyl and N-alkyl groups on stereochemical features of the peroxy-acid–imine reaction. Journal of the Chemical Society Perkin Transactions 2. 923–926. 7 indexed citations
13.
Bucciarelli, Maria, et al.. (1983). Asymmetric synthesis and stereochemical properties of optically active n-sulphonyl-3-aryloxaziridines. Tetrahedron. 39(1). 187–192. 10 indexed citations
14.
15.
Bucciarelli, Maria, Arrigo Forni, Irene Moretti, & Giovanni Torre. (1983). Asymmetric Reduction of Trifluoromethyl and Methyl Ketones by Yeast; An Improved Method. Synthesis. 1983(11). 897–899. 60 indexed citations
16.
Bucciarelli, Maria, Arrigo Forni, Irene Moretti, & Giovanni Torre. (1980). Asymmetric synthesis at nitrogen by oxidation of imines with m-chloroperbenioic acid in the presence of optically active carbinols. Absolute stereochemistry of chiral alcohol-imine-peracid solvates. Journal of the Chemical Society Perkin Transactions 1. 2152–2152. 9 indexed citations
17.
Bucciarelli, Maria, Arrigo Forni, Irene Moretti, & Giovanni Torre. (1978). Asymmetric reduction of trifluoromethyl ketones by actively fermenting yeast. Journal of the Chemical Society Chemical Communications. 456–456. 20 indexed citations
18.
Bucciarelli, Maria, Arrigo Forni, Irene Moretti, & José Garcı́a de la Torre. (1977). Configurational correlations for chiral episulphides and episulphoxides by 1H NMR spectroscopy in optically active solvent. Tetrahedron. 33(9). 999–1002. 5 indexed citations
19.
Bucciarelli, Maria, Arrigo Forni, Irene Moretti, & Giovanni Torre. (1977). Absolute stereochemistry of the peroxy-acid–imine route to optically active oxaziridines. Journal of the Chemical Society Perkin Transactions 2. 1339–1346. 6 indexed citations
20.
Bucciarelli, Maria, Irene Moretti, Giovanni Torre, et al.. (1976). Absolute configuration at the chiral nitrogen atom in an optically active oxaziridine. X-Ray structure of (2S)-(–)-N-(R)-α-methyl-benzyldiphenyloxaziridine. Journal of the Chemical Society Chemical Communications. 60–61. 6 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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