Armen M. Boldi

1.6k total citations
25 papers, 1.4k citations indexed

About

Armen M. Boldi is a scholar working on Organic Chemistry, Molecular Biology and Biotechnology. According to data from OpenAlex, Armen M. Boldi has authored 25 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Organic Chemistry, 7 papers in Molecular Biology and 6 papers in Biotechnology. Recurrent topics in Armen M. Boldi's work include Synthesis and Properties of Aromatic Compounds (10 papers), Chemical Synthesis and Analysis (7 papers) and Synthetic Organic Chemistry Methods (7 papers). Armen M. Boldi is often cited by papers focused on Synthesis and Properties of Aromatic Compounds (10 papers), Chemical Synthesis and Analysis (7 papers) and Synthetic Organic Chemistry Methods (7 papers). Armen M. Boldi collaborates with scholars based in United States, Switzerland and Hungary. Armen M. Boldi's co-authors include François Diederich, Amos B. Smith, John E. Anthony, Carolyn B. Knobler, William H. Moser, Yves Rubin, Linghang Zhuang, Qiyan Lin, Kiyoshi Nakayama and Mark D. McBriar and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Tetrahedron.

In The Last Decade

Armen M. Boldi

25 papers receiving 1.3k citations

Peers

Armen M. Boldi
Toshie Minematsu Japan
Manuel Arnó Spain
Ramón J. Zaragozá Spain
Victor Lee United Kingdom
James A. Ashenhurst Canada
Philip J. Parsons United Kingdom
B. Witulski Germany
Anthony O. King United States
Tsutomu Inokuchi Japan
Ulf Pindur Germany
Toshie Minematsu Japan
Armen M. Boldi
Citations per year, relative to Armen M. Boldi Armen M. Boldi (= 1×) peers Toshie Minematsu

Countries citing papers authored by Armen M. Boldi

Since Specialization
Citations

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

Fields of papers citing papers by Armen M. Boldi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Armen M. Boldi

This figure shows the co-authorship network connecting the top 25 collaborators of Armen M. Boldi. A scholar is included among the top collaborators of Armen M. Boldi 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 Armen M. Boldi. Armen M. Boldi 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.
Smith, Amos B., Qiyan Lin, Victoria A. Doughty, et al.. (2009). Spongipyran synthetic studies. Total synthesis of (+)-spongistatin 2. Tetrahedron. 65(33). 6470–6488. 22 indexed citations
2.
Boldi, Armen M.. (2004). Libraries from natural product-like scaffolds. Current Opinion in Chemical Biology. 8(3). 281–286. 163 indexed citations
3.
Smith, Amos B., Suresh M. Pitram, Armen M. Boldi, et al.. (2003). Multicomponent Linchpin Couplings. Reaction of Dithiane Anions with Terminal Epoxides, Epichlorohydrin, and Vinyl Epoxides:  Efficient, Rapid, and Stereocontrolled Assembly of Advanced Fragments for Complex Molecule Synthesis. Journal of the American Chemical Society. 125(47). 14435–14445. 93 indexed citations
4.
Walters, Michael A., et al.. (2002). Solution-Phase Library Synthesis of Furanoses. Journal of Combinatorial Chemistry. 4(3). 229–238. 16 indexed citations
5.
Dener, Jeffrey M., et al.. (2002). Solid-Phase Synthesis of Trisubsituted Guanidines. Journal of Combinatorial Chemistry. 4(2). 167–174. 24 indexed citations
6.
Smith, Amos B., Victoria A. Doughty, Qiyan Lin, et al.. (2001). The Spongistatins: Architecturally Complex Natural Products-Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment. Angewandte Chemie International Edition. 40(1). 191–195. 95 indexed citations
7.
Smith, Amos B., Victoria A. Doughty, Qiyan Lin, et al.. (2001). The Spongistatins: Architecturally Complex Natural Products—Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment. Angewandte Chemie. 113(1). 197–201. 19 indexed citations
8.
Smith, Amos B., Victoria A. Doughty, Qiyan Lin, et al.. (2001). The Spongistatins: Architecturally Complex Natural Products-Part One: A Formal Synthesis of (+)-Spongistatin 1 by Construction of an Advanced ABCD Fragment Financial support was provided by the National Institutes of Health (National Cancer Institute) through Grant CA-70329, NIH Postdoctoral Fellowships to A.M.B. and W.H.M., a Japan Society for Promotion of Science Fellowship to N.M., and a Royal Society Fulbright Fellowship to V.A.D. We also thank the Daiichi Pharmaceutical Co., Ltd, and the Tanabe Seiyaku Co., Ltd for financial support. Finally we thank Dr. George T. Furst, Dr. Patrick J. Carroll, Dr. Rakesh Kohli, and Mr John Dykins of the University of Pennsylvania Spectroscopic Service Center for assistance in securing and interpreting high-field NMR spectra, X-ray crystal structures, and mass spectra.. PubMed. 40(1). 191–195. 10 indexed citations
9.
Boldi, Armen M., et al.. (2001). Solid-Phase Library Synthesis of Alkoxyprolines. Journal of Combinatorial Chemistry. 3(4). 367–373. 16 indexed citations
10.
Smith, Amos B., Kiyoshi Nakayama, Armen M. Boldi, et al.. (1997). Spongistatin synthetic studies. 3. Construction of the C(1–17) spiroketal. Tetrahedron Letters. 38(50). 8675–8678. 45 indexed citations
11.
Smith, Amos B., Linghang Zhuang, Christopher S. Brook, et al.. (1997). Spongistatin synthetic studies. 2. Assembly of the C(18–28) spiroketal. Tetrahedron Letters. 38(50). 8671–8674. 42 indexed citations
12.
Smith, Amos B. & Armen M. Boldi. (1997). Multicomponent Linchpin Couplings of Silyl Dithianes via Solvent-Controlled Brook Rearrangement. Journal of the American Chemical Society. 119(29). 6925–6926. 108 indexed citations
13.
Smith, Amos B., Linghang Zhuang, Christopher S. Brook, et al.. (1997). Spongistatin synthetic studies. 1. Construction of a C(29–48) subtarget. Tetrahedron Letters. 38(50). 8667–8670. 54 indexed citations
14.
Anthony, John E., Armen M. Boldi, Corinne Boudon, et al.. (1995). Macrocyclic Tetraethynylethene Molecular Scaffolding: Perethynylated aromatic dodecadehydro[18]annulenes, antiaromatic octadehydro[12]annulenes, and expanded radialenes. Helvetica Chimica Acta. 78(4). 797–817. 60 indexed citations
15.
Boldi, Armen M., John E. Anthony, Völker Gramlich, et al.. (1995). Acyclic Tetraethynylethene Molecular Scaffolding: Multinanometer‐sized linearly conjugated rods with the poly(triacetylene) backbone and cross‐conjugated expanded dendralenes. Helvetica Chimica Acta. 78(4). 779–796. 62 indexed citations
16.
Anthony, John E., Armen M. Boldi, Yves Rubin, et al.. (1995). Tetraethynylethenes: Fully cross‐conjugated π‐electron chromophores and molecular scaffolds for all‐carbon networks and carbon‐rich nanomaterials. Helvetica Chimica Acta. 78(1). 13–45. 97 indexed citations
17.
Boldi, Armen M. & François Diederich. (1994). Expanded Radialenes: A Novel Class of Cross‐Conjugated Macrocycles. Angewandte Chemie International Edition in English. 33(4). 468–471. 85 indexed citations
18.
Boldi, Armen M., John E. Anthony, Carolyn B. Knobler, & François Diederich. (1992). Novel Cross‐Conjugated Compounds Derived from Tetraethynylethene. Angewandte Chemie International Edition in English. 31(9). 1240–1242. 42 indexed citations
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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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