William E. Brenzovich

1.5k total citations
16 papers, 1.3k citations indexed

About

William E. Brenzovich is a scholar working on Organic Chemistry, Inorganic Chemistry and Molecular Biology. According to data from OpenAlex, William E. Brenzovich has authored 16 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Organic Chemistry, 3 papers in Inorganic Chemistry and 2 papers in Molecular Biology. Recurrent topics in William E. Brenzovich's work include Catalytic Alkyne Reactions (8 papers), Synthetic Organic Chemistry Methods (6 papers) and Catalytic C–H Functionalization Methods (5 papers). William E. Brenzovich is often cited by papers focused on Catalytic Alkyne Reactions (8 papers), Synthetic Organic Chemistry Methods (6 papers) and Catalytic C–H Functionalization Methods (5 papers). William E. Brenzovich collaborates with scholars based in United States. William E. Brenzovich's co-authors include F. Dean Toste, Aaron D. Lackner, Diego Benítez, E. Tkatchouk, William A. Goddard, Asa D. Melhado, Hunter P. Shunatona, Jean-François Brazeau, Paul G. Bulger and K. C. Nicolaou and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Organic Letters.

In The Last Decade

William E. Brenzovich

15 papers receiving 1.2k citations

Peers

Countries citing papers authored by William E. Brenzovich

Since Specialization

Citations

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

Fields of papers citing papers by William E. Brenzovich

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of William E. Brenzovich

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

All Works

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16 of 16 papers shown

#	Title	Journal	Authors	Indexed citations
1	Aromatic substituent effects in palladium-catalyzed intramolecular olefin oxyarylation reactions	Tetrahedron Letters	Mackenzie W. Sullivan, William E. Brenzovich et al.	1
2	Silica sulfuric acid as a highly efficient catalyst for the synthesis of diarylacetic acids	Synthetic Communications	William E. Brenzovich et al.	8
3	A divergent/convergent approach to dolabriferol: the Kornblum–DeLaMare enantiomeric resolution	Tetrahedron Letters	William E. Brenzovich, Steven T. Staben et al.	8
4	Gold in Total Synthesis: Alkynes as Carbonyl Surrogates	Angewandte Chemie International Edition	William E. Brenzovich	87
5	Gold in der Totalsynthese: Alkine als Carbonylersatz	Angewandte Chemie	William E. Brenzovich	27
6	Gold‐Catalyzed Intramolecular Aminoarylation of Alkenes: CC Bond Formation through Bimolecular Reductive Elimination	Angewandte Chemie International Edition	William E. Brenzovich, Diego Benítez et al.	253
7	Alkylgold complexes by the intramolecular aminoauration of unactivated alkenes	Chemical Science	Rebecca Lyn LaLonde, William E. Brenzovich et al.	152
8	Gold-Catalyzed Oxidative Coupling Reactions with Aryltrimethylsilanes	Organic Letters	William E. Brenzovich, Jean-François Brazeau et al.	136
9	Gold‐Catalyzed Intramolecular Aminoarylation of Alkenes: CC Bond Formation through Bimolecular Reductive Elimination	Angewandte Chemie	William E. Brenzovich, Diego Benítez et al.	82
10	Gold-Catalyzed Oxidative Oxyarylation of Alkenes	Synfacts	F. Dean Toste, Asa D. Melhado et al.	1
11	Gold-Catalyzed Three-Component Coupling: Oxidative Oxyarylation of Alkenes	Journal of the American Chemical Society	Asa D. Melhado, William E. Brenzovich et al.	251
12	Synthesis of iso-epoxy-amphidinolide N and des-epoxy-caribenolide I structures. Initial forays	Organic & Biomolecular Chemistry	K. C. Nicolaou, William E. Brenzovich et al.	45
13	Synthesis of iso-epoxy-amphidinolide N and des-epoxy-caribenolide I structures. Revised strategy and final stages	Organic & Biomolecular Chemistry	K. C. Nicolaou, Paul G. Bulger et al.	62
14	Chemistry and Biology of Diazonamide A: Second Total Synthesis and Biological Investigations	Journal of the American Chemical Society	K. C. Nicolaou, Junliang Hao et al.	145
15	Structure and properties of some cresolphthalein derivatives	Dyes and Pigments	William E. Brenzovich, Christopher J. Abelt et al.	5
16	The synthesis and properties of some carboxy-substituted analogs of butter yellow	Dyes and Pigments	William E. Brenzovich, Ronald J. T. Houk et al.	5

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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