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:

(−)-Neocaryachine, an Antiproliferative Pavine Alkaloid from Cryptocarya laevigata, Induces DNA Double-Strand Breaks
Yuki Suzuki, Yohei Saito, Masuo Goto, et al.
Journal of Natural Products (2017) Vol. 80, Iss. 1, pp. 220-224
Open Access | Times Cited: 26

Showing 1-25 of 26 citing articles:

Copper‐Catalyzed Aerobic Oxidative Cyclization Cascade to Construct Bridged Skeletons: Total Synthesis of (−)‐Suaveoline
Qiuyuan Tan, Yang Zhao, Dan Jiang, et al.
Angewandte Chemie International Edition (2019) Vol. 58, Iss. 19, pp. 6420-6424
Closed Access | Times Cited: 54

Lead/Drug Discovery from Natural Resources
Zhihong Xu, Barrett E. Eichler, Eytan A. Klausner, et al.
Molecules (2022) Vol. 27, Iss. 23, pp. 8280-8280
Open Access | Times Cited: 27

Anti-cancer plants and their therapeutic use as succulent biomedicine capsules
Shibabrata Pattanayak
Exploratory Animal and Medical Research (2023) Vol. 13, Iss. Ethnomedicine Special, pp. 01-50
Open Access | Times Cited: 9

Kleinhospitine E and Cycloartane Triterpenoids from Kleinhovia hospita
Abdul Rahim, Yohei Saito, Katsunori Miyake, et al.
Journal of Natural Products (2018) Vol. 81, Iss. 7, pp. 1619-1627
Open Access | Times Cited: 22

Cytotoxic lignans from Cryptocarya impressinervia
Xiong Ru-qin, Jinhe Jiang, Yegao Chen
Natural Product Research (2019) Vol. 35, Iss. 6, pp. 1019-1023
Closed Access | Times Cited: 20

The application of C–H bond functionalization in the total syntheses of indole natural products
Dongxing Tan, Fu‐She Han
Organic Chemistry Frontiers (2021) Vol. 9, Iss. 4, pp. 1195-1210
Closed Access | Times Cited: 17

Cytotoxic arylalkenyl α,β-unsaturated δ-lactones from Cryptocarya brachythyrsa
Yue Fan, Yu Liu, Yun‐Xia You, et al.
Fitoterapia (2019) Vol. 136, pp. 104167-104167
Closed Access | Times Cited: 17

Unusual acetylated flavonol glucuronides, oxyphyllvonides A−H with renoprotective activities from the fruits of Alpinae oxyphylla
Yue-Tong Zhu, Hong‐Bin Fang, Xiaoning Liu, et al.
Phytochemistry (2023) Vol. 215, pp. 113849-113849
Closed Access | Times Cited: 5

Complex Flavanones from Cryptocarya metcalfiana and Structural Revision of Oboflavanone A
Qian He, Simin Li, Yue Fan, et al.
Journal of Natural Products (2022) Vol. 85, Iss. 6, pp. 1617-1625
Closed Access | Times Cited: 8

Secondary Metabolites, Monoterpene–Polyketides Containing a Spiro[3.5]nonane from Cryptocarya laevigata
Fumika Tsurumi, Yuta Miura, Yohei Saito, et al.
Organic Letters (2018) Vol. 20, Iss. 8, pp. 2282-2286
Open Access | Times Cited: 14

Synthesis of 1,2-Dihydroisoquinolines by a Modified Pomeranz–Fritsch Cyclization
Xiang Ji, Zheng Huang, Jean‐Philip Lumb
The Journal of Organic Chemistry (2019) Vol. 85, Iss. 2, pp. 1062-1072
Open Access | Times Cited: 13

A review of the synthesis of 1,2-dihydroisoquinoline, [2,1-a] isoquinoline and [5,1-a] isoquinoline since 2006
Rahimeh Hajinasiri
Tetrahedron (2021) Vol. 104, pp. 132576-132576
Closed Access | Times Cited: 11

α-Pyrones with glucose uptake-stimulatory activity from the twigs of Cryptocarya wrayi
Xiaona Wang, Xiaodong Kuang, Yong Wang, et al.
Fitoterapia (2022) Vol. 158, pp. 105144-105144
Closed Access | Times Cited: 7

Merging Chemo- and Biocatalysis to Facilitate the Syntheses of Complex Natural Products: Enantioselective Construction of an N-Bridged [3.3.1] Ring System in Indole Terpenoids
Yoshinori Hashimoto, Shingo Harada, Ryosuke Kato, et al.
ACS Catalysis (2022) Vol. 12, Iss. 24, pp. 14990-14998
Closed Access | Times Cited: 6

The Genus Cryptocarya: A Review on Phytochemistry and Pharmacological Activities
Nguyen Manh Ha, Ninh The Son
Chemistry & Biodiversity (2023) Vol. 20, Iss. 3
Closed Access | Times Cited: 3

Copper‐Catalyzed Aerobic Oxidative Cyclization Cascade to Construct Bridged Skeletons: Total Synthesis of (−)‐Suaveoline
Qiuyuan Tan, Yang Zhao, Dan Jiang, et al.
Angewandte Chemie (2019) Vol. 131, Iss. 19, pp. 6486-6490
Closed Access | Times Cited: 9

Cytotoxic α-pyrone derivatives from Cryptocarya yunnanensis
Qian He, Yue Fan, Yu Liu, et al.
Natural Product Research (2020) Vol. 36, Iss. 4, pp. 918-924
Closed Access | Times Cited: 8

Cryptoyunnanones A–H, Complex Flavanones from Cryptocarya yunnanensis
Qian He, Yue Fan, Yu Liu, et al.
Journal of Natural Products (2021) Vol. 84, Iss. 8, pp. 2209-2216
Closed Access | Times Cited: 8

Two new isoquinoline alkaloids from Cryptocarya wrayi and their biological activities
Yun-Lai Liu, Yong Wang, Xiao-Ru He, et al.
Fitoterapia (2021) Vol. 156, pp. 105086-105086
Closed Access | Times Cited: 8

Fatty acid acylated flavonol glycosides from the seeds of Nephelium lappaceum and their nitric oxide suppression activity
Awat Wisetsai, Siwattra Choodej, Nattaya Ngamrojanavanich, et al.
Phytochemistry (2022) Vol. 201, pp. 113262-113262
Closed Access | Times Cited: 4

Extremely Facile Formation of the Pavine Alkaloid Skeleton by the Photoreaction between Isoquinoline and Benzyltrifluoroborate
Yutaka Nishigaichi, Yuuki Ohmuro, Yoshiki Hori, et al.
Chemistry Letters (2019) Vol. 49, Iss. 2, pp. 118-120
Closed Access | Times Cited: 5

Synthetic 3-alkylpyridine alkaloid analogues as a new scaffold against leukemic cell lines: cytotoxic evaluation and mode of action
Fernanda Cristina Gontijo Evangelista, Aline de Freitas Lopes, Silmara Nunes Andrade, et al.
Medicinal Chemistry Research (2019) Vol. 28, Iss. 9, pp. 1567-1578
Closed Access | Times Cited: 3

First Total Synthesis of the Pavine Alkaloid (±)-Neocaryachine and Its Optical Resolution
Yuta Miura, Yohei Saito, Masuo Goto, et al.
Chemical and Pharmaceutical Bulletin (2020) Vol. 68, Iss. 9, pp. 899-902
Open Access | Times Cited: 1

Bioinspired syntheses of cryptoflavanones C and D, oboflavanones A and B, and cryptoyunnanones G and H enabled by an acid-triggered cascade sequence
Anquan Zheng, Sasa Wang, Tingting Zhou, et al.
Organic Chemistry Frontiers (2022) Vol. 9, Iss. 9, pp. 2424-2429
Closed Access | Times Cited: 1

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