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:

A diversity oriented synthesis of natural product inspired molecular libraries
Jyoti Chauhan, Tania Luthra, Rambabu Gundla, et al.
Organic & Biomolecular Chemistry (2017) Vol. 15, Iss. 43, pp. 9108-9120
Closed Access | Times Cited: 22

Showing 22 citing articles:

Natural product drug discovery in the artificial intelligence era
Fernanda I. Saldívar‐González, Victor Daniel Aldas-Bulos, José L. Medina‐Franco, et al.
Chemical Science (2021) Vol. 13, Iss. 6, pp. 1526-1546
Open Access | Times Cited: 132

Current Screening Methodologies in Drug Discovery for Selected Human Diseases
Olga Maria Lage, María C. Ramos, Rita Calisto, et al.
Marine Drugs (2018) Vol. 16, Iss. 8, pp. 279-279
Open Access | Times Cited: 103

Are we seeing a resurgence in the use of natural products for new drug discovery?
Feng Li, Yongli Wang, Dapeng Li, et al.
Expert Opinion on Drug Discovery (2019) Vol. 14, Iss. 5, pp. 417-420
Open Access | Times Cited: 66

Decoding the Structural Diversity: A New Horizon in Antimicrobial Prospecting and Mechanistic Investigation
Ziying Qiu, Rongkun Huang, Yuxuan Wu, et al.
Microbial Drug Resistance (2024) Vol. 30, Iss. 6, pp. 254-272
Closed Access | Times Cited: 2

Diversity-Oriented Synthesis and Chemoinformatic Analysis of the Molecular Diversity of sp3-Rich Morpholine Peptidomimetics
Elena Lenci, Riccardo Innocenti, Gloria Menchi, et al.
Frontiers in Chemistry (2018) Vol. 6
Open Access | Times Cited: 26

Synthesis and evaluation of the performance of a small molecule library based on diverse tropane-related scaffolds
Robert Lowe, Dale Taylor, Kelly Chibale, et al.
Bioorganic & Medicinal Chemistry (2020) Vol. 28, Iss. 9, pp. 115442-115442
Open Access | Times Cited: 17

Diversity‐Oriented Synthesis of Complex Pyrrole‐Based Architectures from Very Simple Starting Materials
Marco Leonardi, Verónica Estévez, Mercedes Villacampa, et al.
Advanced Synthesis & Catalysis (2019) Vol. 361, Iss. 9, pp. 2054-2074
Closed Access | Times Cited: 15

Crystal structure of 3-(methoxycarbonyl)-1-(4-methoxyphenyl)-2,3,4,9- tetrahydro-1H-pyrido[3,4-b]indol-2-ium chloride hydrate, C40H48Cl2N4O9
Yueru Wang, Xiaolin Dang, Changhua Yang, et al.
Zeitschrift für Kristallographie - New Crystal Structures (2024) Vol. 239, Iss. 3, pp. 437-439
Open Access | Times Cited: 1

Nature-inspired synthesis of antibacterial glucovanillin derivatives
Nelson E. Masota, Knut Ohlsen, Lorenz Meinel, et al.
Fitoterapia (2023) Vol. 167, pp. 105475-105475
Closed Access | Times Cited: 2

Iodine‐Catalyzed Metal‐Free Oxidative Ring Opening of 1‐Aryltetrahydro‐β‐carbolines: Facile Synthesis of C‐2 Aroyl and Aryl Methanimino Indole Derivatives
Jyoti Chauhan, Tania Luthra, Subhabrata Sen
European Journal of Organic Chemistry (2018) Vol. 2018, Iss. 34, pp. 4776-4786
Closed Access | Times Cited: 6

Diversity-Oriented Synthesis: Amino Acetophenones as Building Blocks for the Synthesis of Natural Product Analogs
Mathias Eymery, Viet‐Khoa Tran‐Nguyen, Ahcène Boumendjel
Pharmaceuticals (2021) Vol. 14, Iss. 11, pp. 1127-1127
Open Access | Times Cited: 6

The crystal structure of (1S,3R)-1-(4-isopropylphenyl)-3-(methoxycarbonyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-iumchloride monohydrate, C22H27ClN2O3
Jingxiao Zhang, Miao Gu, Xinyu Bai
Zeitschrift für Kristallographie - New Crystal Structures (2022) Vol. 237, Iss. 4, pp. 619-621
Open Access | Times Cited: 4

Crystal structure of methyl 1-(2-bromophenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate, C19H17BrN2O2
Yanli Song, Mo Du, Zhoujing Zhu, et al.
Zeitschrift für Kristallographie - New Crystal Structures (2024) Vol. 239, Iss. 3, pp. 491-493
Open Access

Crystal structure of methyl-1-(p-tolyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate, C20H20N2O2
Yanrong Gao, Xiaolin Dang, Yanjiao Wang, et al.
Zeitschrift für Kristallographie - New Crystal Structures (2024) Vol. 239, Iss. 3, pp. 579-580
Open Access

Crystal structure of (3R)-1-(3,5-dimethoxyphenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate chloride, C21H23ClN2O4
Hongjuan Tong, Xiaona Xu, Zhoujing Zhu, et al.
Zeitschrift für Kristallographie - New Crystal Structures (2024) Vol. 239, Iss. 4, pp. 673-675
Open Access

Crystal structure of methyl-1-(naphthalen-1-yl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b] indole-3-carboxylate, C23H20N2O2
Xiaofeng Yang, Mo Du, Bin Liu, et al.
Zeitschrift für Kristallographie - New Crystal Structures (2024) Vol. 239, Iss. 4, pp. 617-618
Open Access

Crystal structure of methyl (3R)-1-(2-bromo-4-fluorophenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole-3-carboxylate hydrochloride hydrate, C19H19BrClFN2O3
F. W. Wang, Yanjiao Wang, Xiaojuan Han, et al.
Zeitschrift für Kristallographie - New Crystal Structures (2024) Vol. 239, Iss. 4, pp. 767-769
Open Access

Synthesis of C2-Carbonyl Indoles via Visible Light-Induced Oxidative Cleavage of an Aminomethylene Group
Yuzhen Ding, L. Shen, Kangjiang Liang, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 24, pp. 16644-16654
Closed Access | Times Cited: 3

The dual reactivity of Weinreb amides applied to the late-stage divergent functionalisation of meso pyrrolidines
Hamza Boufroura, Laurent Sevaille, Nicolas Gigant, et al.
New Journal of Chemistry (2018) Vol. 42, Iss. 15, pp. 12403-12411
Closed Access | Times Cited: 3

Drug Discovery from Natural Products for Pancreatic Cancer
María C. Ramos, Olga Genilloud, Fernando Reyes, et al.
InTech eBooks (2018)
Open Access | Times Cited: 1

Crystal structure of methyl 2-(2-chloroacetyl)-1-(4-(methoxycarbonyl)phenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b] indole-3-carboxylate, C23H21ClN2O5
Xiaona Xu, Zhoujing Zhu, Bin Liu
Zeitschrift für Kristallographie - New Crystal Structures (2023) Vol. 238, Iss. 2, pp. 355-357
Open Access

Human models as new tools for drug development and precision medicine
Alfred K. Dei-Ampeh, Manuj M. Shah, Gerarda Cappuccio, et al.
Elsevier eBooks (2022), pp. 155-171
Closed Access

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