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OpenAlex Citation Counts

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OpenAlex is a bibliographic catalogue of scientific papers, authors and institutions accessible in open access mode, named after the Library of Alexandria. It's citation coverage is excellent and I hope you will find utility in this listing of citing articles!

If you click the article title, you'll navigate to the article, as listed in CrossRef. If you click the Open Access links, you'll navigate to the "best Open Access location". Clicking the citation count will open this listing for that article. Lastly at the bottom of the page, you'll find basic pagination options.

Requested Article:

Polycyclic indole alkaloid-type compounds by MCR
Wei Wang, Eberhardt Herdtweck, Alexander Dömlingꝉ
Chemical Communications (2009) Vol. 46, Iss. 5, pp. 770-772
Closed Access | Times Cited: 71

Showing 1-25 of 71 citing articles:

Chemistry and Biology Of Multicomponent Reactions
Alexander Dömlingꝉ, Wei Wang, Kan Wang
Chemical Reviews (2012) Vol. 112, Iss. 6, pp. 3083-3135
Open Access | Times Cited: 2255
Multicomponent reactions: advanced tools for sustainable organic synthesis
Răzvan C. Cioc, Eelco Ruijter, Romano V. A. Orrù
Green Chemistry (2014) Vol. 16, Iss. 6, pp. 2958-2975
Closed Access | Times Cited: 1152
Indoles in Multicomponent Processes (MCPs)
Morteza Shiri
Chemical Reviews (2012) Vol. 112, Iss. 6, pp. 3508-3549
Closed Access | Times Cited: 767
Tetrazoles via Multicomponent Reactions
Constantinos G. Neochoritis, Ting Zhao, Alexander Dömlingꝉ
Chemical Reviews (2019) Vol. 119, Iss. 3, pp. 1970-2042
Open Access | Times Cited: 493
To each his own: isonitriles for all flavors. Functionalized isocyanides as valuable tools in organic synthesis
Mariateresa Giustiniano, Andrea Basso, Valentina Mercalli, et al.
Chemical Society Reviews (2016) Vol. 46, Iss. 5, pp. 1295-1357
Closed Access | Times Cited: 364
Consecutive multicomponent reactions for the synthesis of complex molecules
Sanjun Zhi, Xiaoming Ma, Wei Zhang
Organic & Biomolecular Chemistry (2019) Vol. 17, Iss. 33, pp. 7632-7650
Closed Access | Times Cited: 243
Synthesis of polyheterocyclesviamulticomponent reactions
Ilich A. Ibarra, Alejandro Islas‐Jácome, Eduardo González‐Zamora
Organic & Biomolecular Chemistry (2017) Vol. 16, Iss. 9, pp. 1402-1418
Closed Access | Times Cited: 214
Asymmetric Dearomatization of Indoles through a Michael/Friedel–Crafts‐Type Cascade To Construct Polycyclic Spiroindolines
Xiaohu Zhao, Xiaohua Liu, Hongjiang Mei, et al.
Angewandte Chemie International Edition (2015) Vol. 54, Iss. 13, pp. 4032-4035
Closed Access | Times Cited: 182
Recent Advances in Asymmetric Isocyanide‐Based Multicomponent Reactions
Sander S. van Berkel, Berry G. M. Bögels, Marloes A. Wijdeven, et al.
European Journal of Organic Chemistry (2012) Vol. 2012, Iss. 19, pp. 3543-3559
Open Access | Times Cited: 197
Effects of pelletization pressure on the physical and chemical properties of the metal–organic frameworks Cu3(BTC)2 and UiO-66
Gregory W. Peterson, Jared B. DeCoste, T. Grant Glover, et al.
Microporous and Mesoporous Materials (2013) Vol. 179, pp. 48-53
Closed Access | Times Cited: 151
Isocyanide-Based Multicomponent Reactions: Catalyst-Free Stereoselective Construction of Polycyclic Spiroindolines
Xiang Wang, Shun‐Yi Wang, Shun‐Jun Ji
Organic Letters (2013) Vol. 15, Iss. 8, pp. 1954-1957
Closed Access | Times Cited: 113
Upgrading of levulinic acid into diverse N-containing functional chemicals
Zhimin Xue, Dongkun Yu, Xinhui Zhao, et al.
Green Chemistry (2019) Vol. 21, Iss. 20, pp. 5449-5468
Closed Access | Times Cited: 86
The Pictet-Spengler Reaction Updates Its Habits
Andrea Calcaterra, Laura Mangiardi, Giuliano Delle Monache, et al.
Molecules (2020) Vol. 25, Iss. 2, pp. 414-414
Open Access | Times Cited: 71
Skeletal Diverse Synthesis of N-Fused Polycyclic Heterocycles via the Sequence of Ugi-Type MCR and CuI-Catalyzed Coupling/Tandem Pictet–Spengler Reaction
Vikas Tyagi, Shahnawaz Khan, Vikas Bajpai, et al.
The Journal of Organic Chemistry (2012) Vol. 77, Iss. 3, pp. 1414-1421
Closed Access | Times Cited: 91
The asymmetric synthesis of polycyclic 3-spirooxindole alkaloids via the cascade reaction of 2-isocyanoethylindoles
Xiaohu Zhao, Xiaohua Liu, Qian Xiong, et al.
Chemical Communications (2015) Vol. 51, Iss. 89, pp. 16076-16079
Closed Access | Times Cited: 74
Synthesis of polycyclic spiroindolines by highly diastereoselective interrupted Ugi cascade reactions of 3-(2-isocyanoethyl)indoles
Jordy M. Saya, Barry Oppelaar, Răzvan C. Cioc, et al.
Chemical Communications (2016) Vol. 52, Iss. 84, pp. 12482-12485
Closed Access | Times Cited: 61
Current development of β-carboline derived potential antimalarial scaffolds
Preeti Kushwaha, Vipin Kumar, Biswajit Saha
European Journal of Medicinal Chemistry (2023) Vol. 252, pp. 115247-115247
Closed Access | Times Cited: 21
Acid-promoted Cascade Cyclization to Produce Fused-polycyclic Indole Derivatives
Takuya Yokosaka, Hiroki Nakayama, Tetsuhiro Nemoto, et al.
Organic Letters (2013) Vol. 15, Iss. 12, pp. 2978-2981
Closed Access | Times Cited: 56
Asymmetric Dearomatization of Indoles through a Michael/Friedel–Crafts‐Type Cascade To Construct Polycyclic Spiroindolines
Xiaohu Zhao, Xiaohua Liu, Hongjiang Mei, et al.
Angewandte Chemie (2015) Vol. 127, Iss. 13, pp. 4104-4107
Closed Access | Times Cited: 55
Hydrogen‐Bonding‐Promoted Cascade Rearrangement Involving the Enlargement of Two Rings: Efficient Access to Polycyclic Quinoline Derivatives
Wenbin Cao, Shijun Li, Mengmeng Xu, et al.
Angewandte Chemie International Edition (2020) Vol. 59, Iss. 48, pp. 21425-21430
Closed Access | Times Cited: 41
Polycyclic Compounds by Ugi−Pictet−Spengler Sequence
Wei Wang, Sarah Ollio, Eberhardt Herdtweck, et al.
The Journal of Organic Chemistry (2010) Vol. 76, Iss. 2, pp. 637-644
Open Access | Times Cited: 58
Discovery of Highly Potent p53-MDM2 Antagonists and Structural Basis for Anti-Acute Myeloid Leukemia Activities
Yijun Huang, Siglinde Wolf, Barbara Beck, et al.
ACS Chemical Biology (2014) Vol. 9, Iss. 3, pp. 802-811
Open Access | Times Cited: 40
Chemoselective Synthesis of Polycyclic Spiroindolines and Polysubstituted Pyrroles via the Domino Reaction of 2-Isocyanoethylindoles
Xiang Wang, Shun‐Yi Wang, Shun‐Jun Ji
The Journal of Organic Chemistry (2014) Vol. 79, Iss. 18, pp. 8577-8583
Closed Access | Times Cited: 40
Various cyclization scaffolds by a truly Ugi 4-CR
Mantosh K. Sinha, Kareem Khoury, Eberhardt Herdtweck, et al.
Organic & Biomolecular Chemistry (2013) Vol. 11, Iss. 29, pp. 4792-4792
Open Access | Times Cited: 39
A Highly Regio- and Diastereoselective Four-Component Reaction to Construct Polycyclic Bispiroindolines from 2-Isocyanoethylindoles and Isocyanates
Longhai Li, Jiaxin Liu, Min Shi
Organic Letters (2018) Vol. 20, Iss. 22, pp. 7076-7079
Closed Access | Times Cited: 32
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