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:
Dehydroabietane-type bifunctional organocatalysts in asymmetric synthesis: recent progress
Zhenwei Zhang, Liu Shao-wu, Hong-Ping Huang, et al.
RSC Advances (2023) Vol. 13, Iss. 44, pp. 31047-31058
Open Access | Times Cited: 3
Zhenwei Zhang, Liu Shao-wu, Hong-Ping Huang, et al.
RSC Advances (2023) Vol. 13, Iss. 44, pp. 31047-31058
Open Access | Times Cited: 3
Showing 3 citing articles:
Advances in organocatalyzed synthesis of organic compounds
Ayesha Zafar, Muhammad Adnan Iqbal, Ghazala Iram, et al.
RSC Advances (2024) Vol. 14, Iss. 28, pp. 20365-20389
Open Access | Times Cited: 6
Ayesha Zafar, Muhammad Adnan Iqbal, Ghazala Iram, et al.
RSC Advances (2024) Vol. 14, Iss. 28, pp. 20365-20389
Open Access | Times Cited: 6
Bifunctional Photocatalysts Display Proximity-Enhanced Catalytic Activity in Metallaphotoredox C–O Coupling
Luigi Dolcini, Andrea Solida, Daniele Lavelli, et al.
ACS Catalysis (2024), pp. 18651-18659
Open Access | Times Cited: 2
Luigi Dolcini, Andrea Solida, Daniele Lavelli, et al.
ACS Catalysis (2024), pp. 18651-18659
Open Access | Times Cited: 2
Squaramide-catalyzed enantioselective Michael addition of nitromethane to 2-enoylazaarenes: synthesis of chiral azaarene-containing γ-nitroketones
Hong-Ping Huang, Yu-Hang Xie, Xu-Mei Gan, et al.
RSC Advances (2024) Vol. 14, Iss. 28, pp. 20056-20060
Open Access
Hong-Ping Huang, Yu-Hang Xie, Xu-Mei Gan, et al.
RSC Advances (2024) Vol. 14, Iss. 28, pp. 20056-20060
Open Access
