Stephen A. Godleski

1.9k total citations · 1 hit paper
30 papers, 1.3k citations indexed

About

Stephen A. Godleski is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, Stephen A. Godleski has authored 30 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Organic Chemistry, 7 papers in Inorganic Chemistry and 5 papers in Molecular Biology. Recurrent topics in Stephen A. Godleski's work include Synthetic Organic Chemistry Methods (5 papers), Catalytic C–H Functionalization Methods (4 papers) and Asymmetric Synthesis and Catalysis (4 papers). Stephen A. Godleski is often cited by papers focused on Synthetic Organic Chemistry Methods (5 papers), Catalytic C–H Functionalization Methods (4 papers) and Asymmetric Synthesis and Catalysis (4 papers). Stephen A. Godleski collaborates with scholars based in United States, Germany and Israel. Stephen A. Godleski's co-authors include Barry M. Trost, John L. Belletire, Patrick G. McDougal, G. S. PONTICELLO, James P. Springer, James M. Balkovec, Sándor Varga, John J. Baldwin, Marcia E. Christy and J. P. GENET 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

Stephen A. Godleski

30 papers receiving 1.3k citations

Hit Papers

On the use of the O-methy... 1986 2026 1999 2012 1986 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Stephen A. Godleski United States 17 1.0k 303 243 167 95 30 1.3k
A.J.H. Klunder Netherlands 22 1.1k 1.1× 356 1.2× 173 0.7× 166 1.0× 83 0.9× 112 1.5k
Edward M. Burgess United States 23 1.3k 1.3× 350 1.2× 258 1.1× 97 0.6× 73 0.8× 45 1.7k
Gen-ichi Tsuchihashi Japan 26 1.6k 1.6× 486 1.6× 279 1.1× 220 1.3× 121 1.3× 154 2.0k
Rudolph K. Kullnig United States 19 729 0.7× 391 1.3× 206 0.8× 146 0.9× 91 1.0× 45 1.2k
Alvin K. Willard United States 14 928 0.9× 372 1.2× 258 1.1× 172 1.0× 144 1.5× 18 1.4k
Aritsune Kaji Japan 25 2.1k 2.1× 510 1.7× 334 1.4× 250 1.5× 143 1.5× 159 2.5k
John S. Swenton United States 27 2.0k 2.0× 289 1.0× 106 0.4× 118 0.7× 111 1.2× 137 2.2k
Tadamasa Date Japan 20 1.2k 1.2× 346 1.1× 149 0.6× 344 2.1× 114 1.2× 72 1.4k
Gerhard Quinkert Germany 26 1.7k 1.6× 492 1.6× 211 0.9× 99 0.6× 222 2.3× 134 2.2k
Bruce Rickborn United States 27 1.8k 1.8× 354 1.2× 257 1.1× 302 1.8× 180 1.9× 86 2.1k

Countries citing papers authored by Stephen A. Godleski

Since Specialization
Citations

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

Fields of papers citing papers by Stephen A. Godleski

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Stephen A. Godleski. 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 Stephen A. Godleski. The network helps show where Stephen A. Godleski may publish in the future.

Co-authorship network of co-authors of Stephen A. Godleski

This figure shows the co-authorship network connecting the top 25 collaborators of Stephen A. Godleski. A scholar is included among the top collaborators of Stephen A. Godleski 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 Stephen A. Godleski. Stephen A. Godleski 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.
Gould, Ian R., et al.. (2003). Aminosilanes as two-electron donors: A technological application of radical cation chemistry. Canadian Journal of Chemistry. 81(6). 777–788. 16 indexed citations
2.
Jacob, Josemon, et al.. (2002). Cobalt-catalyzed selective conversion of diallylanilines and arylimines to quinolines. Journal of Molecular Catalysis A Chemical. 182-183. 565–570. 14 indexed citations
3.
Jacob, Josemon, et al.. (2001). Nickel-Mediated Selective Carbonylation Routes to Thiocarbamates. Organometallics. 20(5). 1028–1031. 26 indexed citations
4.
Gould, Ian R., et al.. (2001). New approach to silver halide photography using radical cation chemistry. Pure and Applied Chemistry. 73(3). 455–458. 12 indexed citations
5.
Gould, Ian R., Jerome R. Lenhard, Annabel A. Muenter, Stephen A. Godleski, & Samir Farid. (2000). Two-Electron Sensitization:  A New Concept for Silver Halide Photography. Journal of the American Chemical Society. 122(48). 11934–11943. 127 indexed citations
6.
Jones, William D., et al.. (2000). Selective Carbonylation Routes to Thiocarbamates. An Alternative to Phosgene. Organometallics. 19(9). 1661–1669. 40 indexed citations
7.
Godleski, Stephen A. & Edwin B. Villhauer. (1986). Application of a transition-metal-mediated stereospecific Michael reaction equivalent to the synthesis of alloyohimbone. The Journal of Organic Chemistry. 51(4). 486–491. 21 indexed citations
8.
Trost, Barry M., John L. Belletire, Stephen A. Godleski, et al.. (1986). On the use of the O-methylmandelate ester for establishment of absolute configuration of secondary alcohols. The Journal of Organic Chemistry. 51(12). 2370–2374. 536 indexed citations breakdown →
9.
Godleski, Stephen A., et al.. (1985). Platinum and palladium complexes of bicyclo[3.3.1]non-1-ene. Bonding and reactions of strained olefin-transition metal complexes. Organometallics. 4(2). 296–302. 21 indexed citations
10.
Godleski, Stephen A., et al.. (1984). (.pi.-Allyl)palladium complexes of norcamphene. Structure and reactivity. Organometallics. 3(1). 21–28. 21 indexed citations
11.
Godleski, Stephen A., et al.. (1983). Alkoxides as nucleophiles in (.pi.-allyl)palladium chemistry. Synthetic and mechanistic studies. Journal of the American Chemical Society. 105(7). 1964–1969. 60 indexed citations
12.
Godleski, Stephen A., et al.. (1983). Transition-metal-anti-Bredt olefin complexes. Preparation and reactions of platinum(2+) and palladium(2+) complexes of bicyclo[3.3.1]non-1-ene. Organometallics. 2(9). 1254–1257. 4 indexed citations
13.
Godleski, Stephen A., et al.. (1982). MNDO study of phosphine- and amine-substituted silicenium ions. Tetrahedron Letters. 23(43). 4453–4456. 6 indexed citations
14.
Godleski, Stephen A., et al.. (1982). Trimethylsilyl iodide catalyzed spirocyclization of amines. Synthesis of perhydrohistrionicotoxin. The Journal of Organic Chemistry. 47(24). 4820–4822. 11 indexed citations
15.
Apeloig, Yitzhak, et al.. (1981). Stabilization of silicenium ions by second row π-donor substituents.An study.. Tetrahedron Letters. 22(34). 3297–3300. 12 indexed citations
16.
Godleski, Stephen A., et al.. (1981). Palladium assisted synthesis of 1-azaspirocycles. Tetrahedron Letters. 22(24). 2247–2250. 21 indexed citations
17.
Ōsawa, Eiji, Edward M. Engler, Stephen A. Godleski, et al.. (1980). Application of force field calculations to organic chemistry. 10. Bridgehead reactivities of ethanoadamantane. Bromination and solvolysis of bromides. The Journal of Organic Chemistry. 45(6). 984–991. 15 indexed citations
18.
Trost, Barry M., et al.. (1978). Stereocontrolled approach to 1,4-disubstituted 1,3-dienes. The Journal of Organic Chemistry. 43(24). 4559–4564. 22 indexed citations
19.
Godleski, Stephen A., et al.. (1974). Zur Struktur von Brückenkopfderivaten des Homoadamantans. Chemische Berichte. 107(4). 1257–1264. 7 indexed citations
20.
Godleski, Stephen A., et al.. (1974). Syntheses of (D3)-trishomocubane (pentacyclo[6,3,0,02,6,03,10,05,9]undecane) by rearrangement. Journal of the Chemical Society Chemical Communications. 976b–977. 14 indexed citations

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