Andrew McClory

819 total citations
18 papers, 670 citations indexed

About

Andrew McClory is a scholar working on Organic Chemistry, Molecular Biology and Inorganic Chemistry. According to data from OpenAlex, Andrew McClory has authored 18 papers receiving a total of 670 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Organic Chemistry, 9 papers in Molecular Biology and 3 papers in Inorganic Chemistry. Recurrent topics in Andrew McClory's work include Chemical Synthesis and Analysis (6 papers), Synthetic Organic Chemistry Methods (6 papers) and Catalytic C–H Functionalization Methods (4 papers). Andrew McClory is often cited by papers focused on Chemical Synthesis and Analysis (6 papers), Synthetic Organic Chemistry Methods (6 papers) and Catalytic C–H Functionalization Methods (4 papers). Andrew McClory collaborates with scholars based in United States, Switzerland and Canada. Andrew McClory's co-authors include Barry M. Trost, Barry M. Trost, Francis Gosselin, Haiming Zhang, Matthew S. Sigman, David B. Collum, Chong Han, Scott Savage, Ngiap‐Kie Lim and Youla S. Tsantrizos and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and The Journal of Organic Chemistry.

In The Last Decade

Andrew McClory

18 papers receiving 656 citations

Peers

Andrew McClory
Jacqueline C. S. Woo United States
Jun Qin United States
Nancy S. Barta United States
Sarah Y. Fulford United Kingdom
Thomas M. Koenig United States
Jacqueline C. S. Woo United States
Andrew McClory
Citations per year, relative to Andrew McClory Andrew McClory (= 1×) peers Jacqueline C. S. Woo

Countries citing papers authored by Andrew McClory

Since Specialization
Citations

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

Fields of papers citing papers by Andrew McClory

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Andrew McClory. 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 Andrew McClory. The network helps show where Andrew McClory may publish in the future.

Co-authorship network of co-authors of Andrew McClory

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

All Works

18 of 18 papers shown
1.
Xu, Jie, Cheol K. Chung, Andrew McClory, et al.. (2021). Efficient Manufacturing Process for the Selective Estrogen Receptor Degrader GDC-9545 (Giredestrant) via a Crystallization-Driven Diastereoselective Pictet–Spengler Condensation. Organic Process Research & Development. 26(3). 568–582. 5 indexed citations
2.
Remarchuk, Travis, Rémy Angelaud, Diane E. Carrera, et al.. (2019). Manufacture of the PI3K β-Sparing Inhibitor Taselisib. Part 2: Development of a Highly Efficient and Regioselective Late-Stage Process. Organic Process Research & Development. 23(5). 783–793. 6 indexed citations
3.
Savage, Scott, Andrew McClory, Haiming Zhang, et al.. (2018). Synthesis of Selective Estrogen Receptor Degrader GDC-0810 via Stereocontrolled Assembly of a Tetrasubstituted All-Carbon Olefin. The Journal of Organic Chemistry. 83(19). 11571–11576. 18 indexed citations
4.
Lim, Ngiap‐Kie, Scott Savage, Andrew McClory, et al.. (2018). Synthesis of a Selective Estrogen Receptor Degrader via a Stereospecific Elimination Approach. Organic Letters. 20(4). 1114–1117. 11 indexed citations
5.
Sigman, Matthew S., Andrew McClory, Haiming Zhang, Francis Gosselin, & David B. Collum. (2017). Lithium Hexamethyldisilazide-Mediated Enolization of Highly Substituted Aryl Ketones: Structural and Mechanistic Basis of the E/Z Selectivities. Journal of the American Chemical Society. 139(35). 12182–12189. 27 indexed citations
6.
Le, Diane N., Matthew S. Sigman, Andrew McClory, et al.. (2017). Highly Stereoselective Synthesis of Tetrasubstituted Acyclic All-Carbon Olefins via Enol Tosylation and Suzuki–Miyaura Coupling. Journal of the American Chemical Society. 139(31). 10777–10783. 76 indexed citations
7.
Takahashi, Ryan, Shuguang Ma, Qin Yue, et al.. (2016). Absorption, metabolism and excretion of cobimetinib, an oral MEK inhibitor, in rats and dogs. Xenobiotica. 47(1). 50–65. 7 indexed citations
8.
Stumpf, Andreas, et al.. (2016). Development of an Efficient, Safe, and Environmentally Friendly Process for the Manufacture of GDC-0084. Organic Process Research & Development. 20(4). 751–759. 11 indexed citations
9.
McClory, Andrew, W. E. Walker, Jie Xu, et al.. (2015). A Strecker approach to 2-substituted ethyl 5-aminothiazole-4-carboxylates. Tetrahedron Letters. 57(16). 1736–1738. 6 indexed citations
10.
Stockdill, Jennifer L., Douglas C. Behenna, Andrew McClory, & Brian M. Stoltz. (2009). An efficient synthesis of the carbocyclic core of zoanthenol. Tetrahedron. 65(33). 6571–6575. 19 indexed citations
11.
Trost, Barry M. & Andrew McClory. (2008). Metal Vinylidenes as Catalytic Species in Organic Reactions. Chemistry - An Asian Journal. 3(2). 164–194. 177 indexed citations
12.
Trost, Barry M. & Andrew McClory. (2007). Rhodium‐Catalyzed Cycloisomerization: Formation of Indoles, Benzofurans, and Enol Lactones. Angewandte Chemie International Edition. 46(12). 2074–2077. 163 indexed citations
13.
Trost, Barry M. & Andrew McClory. (2007). Rhodium‐Catalyzed Cycloisomerization: Formation of Indoles, Benzofurans, and Enol Lactones. Angewandte Chemie. 119(12). 2120–2123. 46 indexed citations
14.
Trost, Barry M. & Andrew McClory. (2006). Ruthenium-Catalyzed Alkylative Lactonization and Carbocyclization. Organic Letters. 8(17). 3627–3629. 25 indexed citations
15.
Tsantrizos, Youla S., Jean‐Marie Ferland, Andrew McClory, et al.. (2006). Olefin ring-closing metathesis as a powerful tool in drug discovery and development – potent macrocyclic inhibitors of the hepatitis C virus NS3 protease. Journal of Organometallic Chemistry. 691(24-25). 5163–5171. 36 indexed citations
16.
Pagé, Daniel, Andrew McClory, Joanne Butterworth, et al.. (2000). Novel Dmt-Tic dipeptide analogues as selective delta-opioid receptor antagonists. Bioorganic & Medicinal Chemistry Letters. 10(2). 167–170. 18 indexed citations
17.
Li, Chun, Andrew McClory, Elizabeth Wong, & James A. Yergey. (1999). Mass spectrometric analysis of arachidonyl-containing phospholipids in human U937 cells. Journal of Mass Spectrometry. 34(5). 521–536. 5 indexed citations
18.
Tsantrizos, Youla S., Xianshu Yang, & Andrew McClory. (1999). Studies on the Biosynthesis of the Fungal Metabolite Oudenone. 2. Synthesis and Enzymatic Cyclization of an α-Diketone, Open-Chain Precursor into Oudenone in Cultures of Oudemansiella radicata. The Journal of Organic Chemistry. 64(18). 6609–6614. 14 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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