Gregory R. Dake

2.4k total citations
49 papers, 1.9k citations indexed

About

Gregory R. Dake is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Gregory R. Dake has authored 49 papers receiving a total of 1.9k indexed citations (citations by other indexed papers that have themselves been cited), including 43 papers in Organic Chemistry, 14 papers in Molecular Biology and 14 papers in Inorganic Chemistry. Recurrent topics in Gregory R. Dake's work include Synthetic Organic Chemistry Methods (14 papers), Asymmetric Synthesis and Catalysis (11 papers) and Chemical Synthesis and Analysis (10 papers). Gregory R. Dake is often cited by papers focused on Synthetic Organic Chemistry Methods (14 papers), Asymmetric Synthesis and Catalysis (11 papers) and Chemical Synthesis and Analysis (10 papers). Gregory R. Dake collaborates with scholars based in Canada, United States and Germany. Gregory R. Dake's co-authors include Barry M. Trost, Tyler Harrison, Jennifer A. Kozak, Brian O. Patrick, Michaël D. B. Fenster, Derek P. Gates, Julien Dugal‐Tessier, Jacqueline C. S. Woo, James M. Balkovec and Emil R. Koft and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Macromolecules.

In The Last Decade

Gregory R. Dake

49 papers receiving 1.9k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gregory R. Dake Canada	26	1.7k	363	360	172	80	49	1.9k
C. Wade Downey United States	17	1.5k 0.9×	428 1.2×	396 1.1×	81 0.5×	55 0.7×	35	1.7k
Kersten M. Gericke Germany	15	2.5k 1.5×	225 0.6×	490 1.4×	279 1.6×	117 1.5×	26	2.7k
Jun‐ichi Matsuo Japan	27	2.1k 1.2×	344 0.9×	348 1.0×	101 0.6×	80 1.0×	112	2.3k
Tadakatsu Mandai Japan	27	2.1k 1.2×	339 0.9×	481 1.3×	125 0.7×	99 1.2×	113	2.4k
Dhileepkumar Krishnamurthy United States	25	1.8k 1.0×	489 1.3×	429 1.2×	73 0.4×	47 0.6×	89	2.0k
Gordon Brasche Germany	8	3.2k 1.8×	346 1.0×	484 1.3×	179 1.0×	69 0.9×	9	3.3k
Tuyêt Jeffery France	19	2.1k 1.2×	257 0.7×	324 0.9×	103 0.6×	69 0.9×	22	2.2k
Young Ho Rhee South Korea	24	2.0k 1.2×	397 1.1×	381 1.1×	161 0.9×	157 2.0×	84	2.1k
Dipakranjan Mal India	23	1.9k 1.1×	160 0.4×	320 0.9×	259 1.5×	164 2.0×	105	2.2k
Roberto Fernández de la Pradilla Spain	25	2.2k 1.3×	241 0.7×	558 1.6×	79 0.5×	105 1.3×	121	2.4k

Countries citing papers authored by Gregory R. Dake

Since Specialization

Citations

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

Fields of papers citing papers by Gregory R. Dake

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gregory R. Dake. 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 Gregory R. Dake. The network helps show where Gregory R. Dake may publish in the future.

Co-authorship network of co-authors of Gregory R. Dake

This figure shows the co-authorship network connecting the top 25 collaborators of Gregory R. Dake. A scholar is included among the top collaborators of Gregory R. Dake 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 Gregory R. Dake. Gregory R. Dake is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Dake, Gregory R., et al.. (2020). Nickel‐Catalyzed Arylative Additions on 2‐Alkynyl‐N‐Arylsulfonylanilides to Construct Functionalized Indoles. European Journal of Organic Chemistry. 2020(6). 744–748. 7 indexed citations

Knox, Kerry J., Elizabeth A. L. Gillis, & Gregory R. Dake. (2018). A positive student experience of collaborative project work in upper-year undergraduate chemistry. Chemistry Education Research and Practice. 20(2). 340–357. 8 indexed citations

Serin, Spencer C., Gregory R. Dake, & Derek P. Gates. (2016). Phosphaalkene-oxazoline copolymers with styrene as chiral ligands for rhodium(i). Dalton Transactions. 45(13). 5659–5666. 13 indexed citations

Serin, Spencer C., Brian O. Patrick, Gregory R. Dake, & Derek P. Gates. (2014). Reaction of an Enantiomerically Pure Phosphaalkene-Oxazoline with MeM Nucleophiles (M = Li and MgBr): Stereoselectivity and Noninnocence of the P-Mesityl Substituent. Organometallics. 33(24). 7215–7222. 5 indexed citations

Dake, Gregory R., et al.. (2013). Paradoxical Activation of an Inwardly Rectifying Potassium Channel Mutant by Spermine: "(B)locking" Open the Bundle Crossing Gate. Molecular Pharmacology. 84(4). 572–581. 2 indexed citations

Andersen, Raymond J., et al.. (2013). Total Synthesis of Cladoniamide G. Organic Letters. 15(5). 1152–1154. 28 indexed citations

Dugal‐Tessier, Julien, et al.. (2012). Enantiomerically Pure Phosphaalkene–Oxazolines (PhAk‐Ox): Synthesis, Scope and Copolymerization with Styrene. Chemistry - A European Journal. 18(20). 6349–6359. 20 indexed citations

Dake, Gregory R.. (2012). Enamides and Related Functional Groups as Nucleophilic Components in Ring-Forming Processes Catalyzed by Electrophilic Metal Salts. Synlett. 23(6). 814–824. 35 indexed citations

Dugal‐Tessier, Julien, et al.. (2010). Synthesis of functional phosphines with ortho‐substituted aryl groups: 2‐RC₆H₄PH₂ and 2‐RC₆H₄P(SiMe₃)₂ (R = 2‐i‐Pr‐ or 2‐t‐Bu‐). Heteroatom Chemistry. 21(4). 265–270. 5 indexed citations

10.

Kozak, Jennifer A., et al.. (2009). Enamides and Enesulfonamides as Nucleophiles: Formation of Complex Ring Systems through a Platinum(II)-Catalyzed Addition/Friedel−Crafts Pathway. The Journal of Organic Chemistry. 74(18). 6929–6935. 26 indexed citations

11.

Kozak, Jennifer A. & Gregory R. Dake. (2008). Total Synthesis of (+)‐Fawcettidine. Angewandte Chemie International Edition. 47(22). 4221–4223. 94 indexed citations

12.

Dugal‐Tessier, Julien, Gregory R. Dake, & Derek P. Gates. (2008). Chiral Ligand Design: A Bidentate Ligand Incorporating an Acyclic Phosphaalkene. Angewandte Chemie International Edition. 47(42). 8064–8067. 27 indexed citations

13.

Wilson, Michael, Jacqueline C. S. Woo, & Gregory R. Dake. (2006). A Synthetic Approach toward Nitiol: Construction of Two 1,22-Dihydroxynitianes. The Journal of Organic Chemistry. 71(11). 4237–4245. 31 indexed citations

14.

Fenster, Michaël D. B. & Gregory R. Dake. (2004). An Asymmetric Formal Synthesis of Fasicularin. Chemistry - A European Journal. 11(2). 639–649. 35 indexed citations

15.

Harrison, Tyler & Gregory R. Dake. (2004). Pt(II) or Ag(I) Salt Catalyzed Cycloisomerizations and Tandem Cycloadditions Forming Functionalized Azacyclic Arrays. Organic Letters. 6(26). 5023–5026. 76 indexed citations

16.

Dake, Gregory R., et al.. (2004). Nucleophilic additions of lactam-derived enol triflates to aldehydes mediated by nickel(II) and chromium(II) salts. Canadian Journal of Chemistry. 82(2). 139–144. 3 indexed citations

17.

Dake, Gregory R., et al.. (2004). Investigations of α-Siloxy−Epoxide Ring Expansions Forming 1-Azaspirocyclic Ketones. The Journal of Organic Chemistry. 69(17). 5676–5683. 28 indexed citations

18.

Fenster, Michaël D. B. & Gregory R. Dake. (2003). A Formal Construction of Fasicularin. Organic Letters. 5(23). 4313–4316. 34 indexed citations

19.

Wilson, Michael & Gregory R. Dake. (2001). Stereocontrolled Construction of the A-Ring of Nitiol Using a Pauson−Khand Cycloaddition−Ring Fragmentation Strategy. Organic Letters. 3(13). 2041–2044. 8 indexed citations

20.

Stork, Gilbert, Deqiang Niu, Emil R. Koft, et al.. (2001). The First Stereoselective Total Synthesis of Quinine. Journal of the American Chemical Society. 123(14). 3239–3242. 148 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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