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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:

Total Synthesis of Yuzurine-type Alkaloid Daphgraciline
Lixuan Li, Long Min, Tian-Bing Yao, et al.
Journal of the American Chemical Society (2022) Vol. 144, Iss. 41, pp. 18823-18828
Closed Access | Times Cited: 25

Showing 25 citing articles:

Total Synthesis of (±)- and (−)-Daphnillonin B
Yun-Peng Zou, Zheng-Lin Lai, Mengwei Zhang, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 20, pp. 10998-11004
Closed Access | Times Cited: 24
Enantioselective Total Synthesis of (−)-Daphenylline
Bing-Lu Wu, Jian-Neng Yao, Xiang-Xi Long, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 2, pp. 1262-1268
Closed Access | Times Cited: 11
Recent advancements in the chemistry of Diels–Alder reaction for total synthesis of natural products: a comprehensive review (2020–2023)
A. C. Rana, Anupam Mishra, Satish Kumar Awasthi
RSC Advances (2025) Vol. 15, Iss. 6, pp. 4496-4525
Open Access | Times Cited: 1
Total Syntheses of Rhodomollins A and B
Weizhao Zhao, Duo Zhang, Yuran Wang, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 49, pp. 27160-27166
Closed Access | Times Cited: 15
Divergent Total Syntheses of (−)‐Daphnezomines A and B and (+)‐Dapholdhamine B
Shaobin Su, Chengcheng Lin, Hongbin Zhai
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 23
Closed Access | Times Cited: 14
Strategies for constructing seven-membered rings: Applications in natural product synthesis
Peng Chen, Lijuan Liang, Yufei Zhu, et al.
Chinese Chemical Letters (2023) Vol. 35, Iss. 6, pp. 109229-109229
Closed Access | Times Cited: 11
Molecular Complexity-Inspired Synthetic Strategies toward the Calyciphylline A-Type Daphniphyllum Alkaloids Himalensine A and Daphenylline
Brandon A. Wright, Taku Okada, Alessio Regni, et al.
Journal of the American Chemical Society (2024)
Closed Access | Times Cited: 4
Forging the Tetracyclic Core Framework of Daphlongamine B Enabled by a Peripheral Derivation of the Aza-Angular Triquinane Strategy
Huijuanzi Rao, Binbin Deng, Sun Peng, et al.
Organic Letters (2025)
Closed Access
Recent Progress in the Total Synthesis of Daphniphyllum Alkaloids
Hai-Kang Mao, Jing Xu
Chinese Journal of Organic Chemistry (2025) Vol. 45, Iss. 3, pp. 866-866
Closed Access
Synthesis of the AB Ring System of Daphniphyllum Alkaloid Daphniglaucin C
Xiaofeng Zhang, Aggeliki Roumana, Hai-Kang Mao, et al.
Chinese Journal of Organic Chemistry (2025) Vol. 45, Iss. 3, pp. 925-925
Closed Access
Diverse synthesis of bridged bicyclo[3.2.1]octa-2,6-diene and tricyclo[3.2.1.0²,7] oct-3-ene frameworks via stepwise cascade reactions
Z. Zheng, Mu-Qiu Chen, Jing Zhou, et al.
Chinese Chemical Letters (2025), pp. 111202-111202
Closed Access
Asymmetric total synthesis of polycyclic xanthenes and discovery of a WalK activator active against MRSA
Min-Jing Cheng, Yan-Yi Wu, Hao Zeng, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2
Total Synthesis of Daphniphyllum Alkaloids: (+)-Daphlongamine E, (+)-Calyciphylline R, and (–)-10-Deoxydaphnipaxianine A
Yan Zhang, Yuye Chen, Jing Xu
Synthesis (2024) Vol. 56, Iss. 08, pp. 1273-1284
Closed Access | Times Cited: 2
Development of water-soluble phenazine-2,3-diol-based photosensitizers for singlet oxygen generation
Kazunori Yagi, Kazuki Ohira, Keita Yamana, et al.
Organic & Biomolecular Chemistry (2023) Vol. 21, Iss. 25, pp. 5194-5202
Open Access | Times Cited: 4
Total synthesis of a putative yuzurimine-type Daphniphyllum alkaloid C14‑epi-deoxycalyciphylline H
Jingping Hu, Jing Xu
Chinese Chemical Letters (2023) Vol. 35, Iss. 4, pp. 108733-108733
Closed Access | Times Cited: 4
Grignard Reaction: An ‘Old-Yet-Gold’ synthetic gadget toward the synthesis of natural Products: A review
Muhammad Haroon, Sajjad Ahmad, Ameer Fawad Zahoor, et al.
Arabian Journal of Chemistry (2024) Vol. 17, Iss. 5, pp. 105715-105715
Open Access | Times Cited: 1
Synthetic Study toward Daphnimacropodines
Hai-Kang Mao, Qian Wang, Sujun Xie, et al.
Organic Letters (2024)
Closed Access | Times Cited: 1
Synthetic Studies Toward Daphnezomines A and B
Ming Yang, Chenguang Dou
Synlett (2023)
Closed Access | Times Cited: 2
Synthetic Studies to exo‐Ring‐Junction based Fused 5/5/n‐Tricyclic Systems: Access to A, B, C‐Ring System of Longeracinphyllin A, Himalenine D, and Daphnipaxiamine A.
Sambasivarao Kotha, Arpit Agrawal, Ramakrishna Reddy Keesari
Asian Journal of Organic Chemistry (2023) Vol. 12, Iss. 6
Closed Access | Times Cited: 2
Enantioselective Construction of Polycyclic Chromanes through Organocatalytic Sequential Quintuple Reaction via One‐Pot Step‐Wise Procedure
Jie Wang, Hang Qin, Yali Song, et al.
Chinese Journal of Chemistry (2024) Vol. 42, Iss. 18, pp. 2197-2202
Closed Access
[5 + 2] and [6 + 2] Cycloaddition Reaction of Alkenes, Alkynes, Allenes and 1,3-Dienes
Hanfeng Ding, Kai Gao, Yuan Qu, et al.
Elsevier eBooks (2024)
Closed Access
The Latest Progress in the Chemistry of Daphniphyllum Alkaloids
Lujuan Chen, Chao Lv, Yan Meng, et al.
Molecules (2024) Vol. 29, Iss. 23, pp. 5498-5498
Open Access
Construction of the [7–5–5] Tricyclic Core of Daphniphyllum Alkaloids via a Cationic Cascade Reaction
Daisuke Nakajima, Satoshi Yokoshima
Organic Letters (2022) Vol. 24, Iss. 51, pp. 9520-9524
Closed Access | Times Cited: 2
Divergent Total Syntheses of (−)‐Daphnezomines A and B and (+)‐Dapholdhamine B
Shaobin Su, Chengcheng Lin, Hongbin Zhai
Angewandte Chemie (2023) Vol. 135, Iss. 23
Open Access
Total Synthesis of (±)-Daphgraciline
Erick M. Carreira, Sven M. Papidocha
Synfacts (2022) Vol. 19, Iss. 01, pp. 0001-0001
Open Access
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