Andrew E. Greene

6.6k total citations
166 papers, 5.1k citations indexed

About

Andrew E. Greene is a scholar working on Organic Chemistry, Molecular Biology and Pharmacology. According to data from OpenAlex, Andrew E. Greene has authored 166 papers receiving a total of 5.1k indexed citations (citations by other indexed papers that have themselves been cited), including 127 papers in Organic Chemistry, 42 papers in Molecular Biology and 26 papers in Pharmacology. Recurrent topics in Andrew E. Greene's work include Asymmetric Synthesis and Catalysis (52 papers), Synthetic Organic Chemistry Methods (44 papers) and Oxidative Organic Chemistry Reactions (19 papers). Andrew E. Greene is often cited by papers focused on Asymmetric Synthesis and Catalysis (52 papers), Synthetic Organic Chemistry Methods (44 papers) and Oxidative Organic Chemistry Reactions (19 papers). Andrew E. Greene collaborates with scholars based in France, Spain and Brazil. Andrew E. Greene's co-authors include J. N. DENIS, Alice Kanazawa, Albert Moyano, Jean‐Pierre Deprés, Arlene G. Corrêa, Marie Jacqueline Luche, Florence Charbonnier, Philippe Delair, Jean‐François Poisson and M. B. M. DE AZEVEDO and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Accounts of Chemical Research.

In The Last Decade

Andrew E. Greene

166 papers receiving 4.8k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Andrew E. Greene France 40 4.1k 1.2k 666 518 515 166 5.1k
H. M. R. Hoffmann Germany 36 5.9k 1.4× 1.3k 1.1× 220 0.3× 436 0.8× 578 1.1× 280 6.6k
Edward Piers Canada 34 3.5k 0.8× 1.1k 0.9× 233 0.3× 409 0.8× 350 0.7× 202 4.3k
Philip Magnus United States 44 6.0k 1.5× 1.2k 1.0× 169 0.3× 438 0.8× 666 1.3× 250 6.7k
P. L. Fuchs United States 40 4.7k 1.1× 1.7k 1.4× 185 0.3× 366 0.7× 356 0.7× 234 6.1k
Derrick L. J. Clive Canada 33 4.1k 1.0× 1.0k 0.8× 149 0.2× 414 0.8× 442 0.9× 217 4.8k
Douglass F. Taber United States 44 5.6k 1.4× 1.2k 1.0× 167 0.3× 460 0.9× 806 1.6× 222 6.9k
Erik J. Sorensen United States 47 5.7k 1.4× 2.4k 2.0× 1.7k 2.6× 1.3k 2.4× 626 1.2× 133 7.9k
Chisato Mukai Japan 39 4.3k 1.0× 699 0.6× 210 0.3× 415 0.8× 497 1.0× 235 5.0k
Yasumasa Hamada Japan 44 5.6k 1.4× 2.4k 1.9× 206 0.3× 706 1.4× 1.5k 2.8× 237 6.8k
Daniel Romo United States 51 5.1k 1.2× 2.4k 1.9× 201 0.3× 782 1.5× 583 1.1× 206 7.2k

Countries citing papers authored by Andrew E. Greene

Since Specialization
Citations

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

Fields of papers citing papers by Andrew E. Greene

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew E. Greene. 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 Andrew E. Greene. The network helps show where Andrew E. Greene may publish in the future.

Co-authorship network of co-authors of Andrew E. Greene

This figure shows the co-authorship network connecting the top 25 collaborators of Andrew E. Greene. A scholar is included among the top collaborators of Andrew E. Greene 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 Andrew E. Greene. Andrew E. Greene 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.
Lesage, Denis, Anne Milet, Antony Memboeuf, et al.. (2014). The Pauson–Khand Mechanism Revisited: Origin of CO in the Final Product. Angewandte Chemie International Edition. 53(7). 1939–1942. 25 indexed citations
2.
Ceccon, Julien, Grégory Danoun, Andrew E. Greene, & Jean‐François Poisson. (2009). Asymmetric synthesis of (+)-castanospermine through enol ether metathesis–hydroboration/oxidation. Organic & Biomolecular Chemistry. 7(10). 2029–2029. 37 indexed citations
3.
Prévost, Grégoire, et al.. (2008). Synthesis and bioevaluation of 22-hydroxyacuminatine analogs. Bioorganic & Medicinal Chemistry Letters. 18(6). 2143–2146. 19 indexed citations
4.
Koóš, Peter, et al.. (2008). Approach to the hyacinthacines: first non-chiral pool synthesis of (+)-hyacinthacine A1. Organic & Biomolecular Chemistry. 6(7). 1170–1170. 39 indexed citations
5.
Anderson, R. J., et al.. (2006). Novel, efficient total synthesis of natural 20(S)-camptothecin. Organic & Biomolecular Chemistry. 4(20). 3757–3757. 21 indexed citations
6.
Bruin, Theodorus de, et al.. (2006). First C–C bond formation in the Pauson–Khand reaction: Influence of carbon–carbon triple bond polarization on regiochemistry. Journal of Organometallic Chemistry. 691(20). 4281–4288. 30 indexed citations
7.
Milet, Anne, et al.. (2005). Reaction of nitrones with silyl ketene acetals: A DFT study. Journal of Computational Chemistry. 27(2). 157–162. 18 indexed citations
8.
Valle, Carlos Pérez del, et al.. (2005). Lewis Base Promoters in the Pauson–Khand Reaction: A Different Scenario. Angewandte Chemie International Edition. 44(35). 5717–5719. 20 indexed citations
9.
Carret, Sébastien, Aurélien Blanc, Yoann Coquerel, et al.. (2005). Approach to the Blues: A Highly Flexible Route to the Azulenes. Angewandte Chemie International Edition. 44(32). 5130–5133. 46 indexed citations
10.
Delair, Philippe, et al.. (2005). New Asymmetric Approach to Natural Pyrrolizidines:  Synthesis of (+)-Amphorogynine A, (+)-Amphorogynine D, and (+)-Retronecine. The Journal of Organic Chemistry. 70(21). 8352–8363. 28 indexed citations
11.
Kanazawa, Alice, et al.. (2003). Highly Stereocontrolled Synthesis of Natural Barbacenic Acid, Novel Bisnorditerpene from Barbacenia flava. The Journal of Organic Chemistry. 68(10). 3831–3837. 14 indexed citations
12.
Greene, Andrew E., et al.. (2003). A Modular Approach to Oxoindolizino Quinolines: Efficient Synthesis of Mappicine Ketone (Nothapodytine B). Angewandte Chemie International Edition. 42(41). 5059–5061. 23 indexed citations
13.
Konya, D., Christian Philouze, Yves Gimbert, & Andrew E. Greene. (2002). New electron-deficient chiral phosphines: (4R,5R)-1,3-bis(trifluoromethanesulfonyl)perhydro-1,3,2-benzodiazaphosphol-2-yl] substituted amines. Acta Crystallographica Section C Crystal Structure Communications. 58(2). o108–o111. 2 indexed citations
14.
Gimbert, Yves, et al.. (2002). Synthetic Approach to Hypoxyxylerone, Novel Inhibitor of Topoisomerase I. Organic Letters. 4(18). 3139–3142. 26 indexed citations
15.
Kanazawa, Alice, et al.. (2000). Efficient, Highly Enantioselective Synthesis of Selina-1,3,7(11)-trien-8-one, a Major Component of the Essential Oil of Eugenia uniflora. Journal of Natural Products. 63(9). 1292–1294. 24 indexed citations
16.
Hamelin, Olivier, Yanyun Wang, Jean‐Pierre Deprés, & Andrew E. Greene. (2000). The First Entry to Complex Bakkanes: A Highly Effective Retroaldol–Aldol-Based Approach to (−)-Bakkenolides III, B, C, and H. Angewandte Chemie International Edition. 39(23). 4314–4316. 20 indexed citations
17.
Mekouar, Khalid, et al.. (2000). New Pyridone Approach:  Total Synthesis of Mappicine Ketone (Nothapodytine B). The Journal of Organic Chemistry. 65(17). 5212–5215. 24 indexed citations
18.
Delair, Philippe, Nina Kann, & Andrew E. Greene. (1994). Synthesis (in ent-form) of a novel jalcaguaianolide from Ferula arrigonii Bocchieri. Journal of the Chemical Society Perkin Transactions 1. 1651–1651. 11 indexed citations
19.
Greene, Andrew E., Gerald R. Girard, & James F. Kerwin. (1975). Enone transposition in prostaglandins - a useful sequence for the synthesis of 13-hydroxyprostanoic acid analogs. Tetrahedron Letters. 16(11). 937–938. 2 indexed citations
20.
Greene, Andrew E., et al.. (1972). A new approach to α-methylene-γ-butyrolactones. Synthesis of (−)-frullanolide.. Tetrahedron Letters. 13(24). 2489–2492. 10 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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