Daniel T. Longone

515 total citations
33 papers, 371 citations indexed

About

Daniel T. Longone is a scholar working on Organic Chemistry, Molecular Biology and Materials Chemistry. According to data from OpenAlex, Daniel T. Longone has authored 33 papers receiving a total of 371 indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Organic Chemistry, 8 papers in Molecular Biology and 6 papers in Materials Chemistry. Recurrent topics in Daniel T. Longone's work include Synthesis and Properties of Aromatic Compounds (17 papers), DNA and Nucleic Acid Chemistry (8 papers) and Synthetic Organic Chemistry Methods (4 papers). Daniel T. Longone is often cited by papers focused on Synthesis and Properties of Aromatic Compounds (17 papers), DNA and Nucleic Acid Chemistry (8 papers) and Synthetic Organic Chemistry Methods (4 papers). Daniel T. Longone collaborates with scholars based in United States. Daniel T. Longone's co-authors include A. T. Blomquist, Daniel T. Glatzhofer, John A. Gladysz, Seli̇m H. Küsefoǧlu, William D. Wright, C. S. Marvel, Philip S. Hammond, G. Smith, Joseph Wolinsky and Yvonne C. Meinwald and has published in prestigious journals such as Journal of the American Chemical Society, The Journal of Organic Chemistry and Tetrahedron Letters.

In The Last Decade

Daniel T. Longone

33 papers receiving 349 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniel T. Longone United States 12 300 80 66 48 41 33 371
Kenneth F. King United States 7 232 0.8× 54 0.7× 47 0.7× 38 0.8× 44 1.1× 9 348
S. Theodoropulos United States 10 247 0.8× 64 0.8× 69 1.0× 21 0.4× 38 0.9× 10 345
S. Yaroslavsky Israel 11 245 0.8× 110 1.4× 35 0.5× 57 1.2× 55 1.3× 20 370
John P. Idoux United States 11 322 1.1× 77 1.0× 61 0.9× 43 0.9× 29 0.7× 44 415
H. E. Winberg 6 292 1.0× 32 0.4× 57 0.9× 39 0.8× 57 1.4× 7 396
A. E. SIEGRIST Switzerland 12 336 1.1× 60 0.8× 92 1.4× 36 0.8× 61 1.5× 25 433
Ennio Ciuffarin Italy 12 280 0.9× 59 0.7× 25 0.4× 72 1.5× 64 1.6× 27 359
WILHELM WENNER Switzerland 11 181 0.6× 64 0.8× 46 0.7× 34 0.7× 19 0.5× 23 293
D. A. Barr United Kingdom 12 406 1.4× 91 1.1× 62 0.9× 26 0.5× 18 0.4× 18 512
B. H. Klanderman United States 12 250 0.8× 24 0.3× 118 1.8× 98 2.0× 73 1.8× 16 414

Countries citing papers authored by Daniel T. Longone

Since Specialization
Citations

This map shows the geographic impact of Daniel T. Longone'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 Daniel T. Longone with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Daniel T. Longone more than expected).

Fields of papers citing papers by Daniel T. Longone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Daniel T. Longone. 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 Daniel T. Longone. The network helps show where Daniel T. Longone may publish in the future.

Co-authorship network of co-authors of Daniel T. Longone

This figure shows the co-authorship network connecting the top 25 collaborators of Daniel T. Longone. A scholar is included among the top collaborators of Daniel T. Longone 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 Daniel T. Longone. Daniel T. Longone 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.
Longone, Daniel T. & Daniel T. Glatzhofer. (1986). Cyclopolymerization of (E,E) ‐ [6.2]paracyclophane‐1,5‐diene. Journal of Polymer Science Part A Polymer Chemistry. 24(8). 1725–1733. 26 indexed citations
2.
Glatzhofer, Daniel T. & Daniel T. Longone. (1986). 4,14-divinyl-(,)-[4.4]paracyclophane-1, 11-diene. An unusual product from a 1,10-Hofmann elimination. Tetrahedron Letters. 27(49). 5923–5926. 2 indexed citations
3.
Glatzhofer, Daniel T. & Daniel T. Longone. (1983). A 1,10-hofmann elimination. Synthesis of a [6.6]paracyclopane tetraene. Tetrahedron Letters. 24(41). 4413–4416. 5 indexed citations
4.
Hammond, Philip S. & Daniel T. Longone. (1978). Synthesis of [4.2]cyclophanes. Tetrahedron Letters. 19(5). 415–418. 8 indexed citations
5.
Longone, Daniel T., Seli̇m H. Küsefoǧlu, & John A. Gladysz. (1977). A convenient synthesis of [3.3]paracyclophane. The Journal of Organic Chemistry. 42(16). 2787–2788. 24 indexed citations
6.
Longone, Daniel T., et al.. (1974). A vinylog of--xylylene. Synthesis of [2.6]paracyclophane. Tetrahedron Letters. 15(36). 3229–3230. 7 indexed citations
7.
Longone, Daniel T., et al.. (1970). 1,2-diphenylcyclopropene. Tetrahedron Letters. 11(13). 1017–1019. 17 indexed citations
8.
Longone, Daniel T., et al.. (1970). Multilayered [2.2]paracyclophane. Synthesis and properties. Journal of the American Chemical Society. 92(4). 994–998. 32 indexed citations
9.
Longone, Daniel T., et al.. (1969). The reaction of cyclopropenyl cations with cyclopropenes. Tetrahedron Letters. 10(60). 5311–5313. 3 indexed citations
10.
Longone, Daniel T. & William D. Wright. (1969). Oxygenation of cyclopropyllithiums: a convenient synthesis of cyclopropanols. Tetrahedron Letters. 10(33). 2859–2862. 9 indexed citations
11.
Longone, Daniel T., et al.. (1969). [2](1,4)-Benzeno-[2](1,4)-triptycenophane: nuclear magnetic resonance evidence of a skew [2,2]-paracyclophane moiety. Journal of the Chemical Society D Chemical Communications. 1358–1358. 4 indexed citations
12.
Longone, Daniel T., et al.. (1968). Unusually high pch coupling constants in cyclopropenylphosphonium salts. Tetrahedron Letters. 9(55). 5815–5818. 2 indexed citations
13.
Longone, Daniel T., et al.. (1967). Conversion of cyclopropyl bromides to cyclopropyloxy derivatives. Tetrahedron Letters. 8(49). 4941–4944. 2 indexed citations
14.
Longone, Daniel T., et al.. (1964). Paracyclophanes. IV. A Multilayered [2.2]Paracyclophane. Journal of the American Chemical Society. 86(18). 3898–3899. 23 indexed citations
15.
Longone, Daniel T., et al.. (1963). A Nonaromatic Route to a Paracyclophane: A Study of the 1,2,4,5-Tetramethylenecyclohexane to Tetramethyl[2.2]paracyclophane Conversion. Journal of the American Chemical Society. 85(21). 3436–3443. 10 indexed citations
16.
Longone, Daniel T. & G. Smith. (1962). Tetracyanoethylene as an aromatizing agent. Tetrahedron Letters. 3(5). 205–207. 8 indexed citations
17.
Longone, Daniel T., et al.. (1962). A Non-Aromatic Route to a Paracyclophane. Journal of the American Chemical Society. 84(8). 1507–1509. 20 indexed citations
18.
Marvel, C. S., et al.. (1959). Polymerization of β‐pinene with ziegler‐type catalysts. Journal of Polymer Science. 40(137). 551–555. 16 indexed citations
19.
Blomquist, A. T. & Daniel T. Longone. (1959). Synthesis of Cyclopropane Derivatives. Precursors for Dimethylenecyclopropane and Trimethylenecyclopropane. Journal of the American Chemical Society. 81(8). 2012–2017. 34 indexed citations
20.
Blomquist, A. T. & Daniel T. Longone. (1957). 1,2-Dimethylenecyclohexane. Synthesis and Polymerization1. Journal of the American Chemical Society. 79(14). 3916–3919. 17 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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