OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Recent Advances in Diversity Oriented Synthesis through Isatin‐based Multicomponent Reactions
Yunyun Liu, Hang Wang, Jie‐Ping Wan
Asian Journal of Organic Chemistry (2013) Vol. 2, Iss. 5, pp. 374-386
Closed Access | Times Cited: 207

Showing 1-25 of 207 citing articles:

Spirooxindoles: Promising scaffolds for anticancer agents
Bin Yu, De‐Quan Yu, Hong‐Min Liu
European Journal of Medicinal Chemistry (2014) Vol. 97, pp. 673-698
Closed Access | Times Cited: 756

Recent advances in the synthesis of biologically active spirooxindoles
Maria M. M. Santos
Tetrahedron (2014) Vol. 70, Iss. 52, pp. 9735-9757
Closed Access | Times Cited: 368

Stereoselective synthesis and applications of spirocyclic oxindoles
Alexander J. Boddy, James A. Bull
Organic Chemistry Frontiers (2021) Vol. 8, Iss. 5, pp. 1026-1084
Open Access | Times Cited: 253

Catalyst-Free, Visible-Light Promoted One-Pot Synthesis of Spirooxindole-Pyran Derivatives in Aqueous Ethyl Lactate
Mo Zhang, Qiuyang Fu, Ge Gao, et al.
ACS Sustainable Chemistry & Engineering (2017) Vol. 5, Iss. 7, pp. 6175-6182
Closed Access | Times Cited: 174

The asymmetric synthesis of CF3-containing spiro[pyrrolidin-3,2′-oxindole] through the organocatalytic 1,3-dipolar cycloaddition reaction
Mingxia Ma, Yuan‐Yuan Zhu, Quantao Sun, et al.
Chemical Communications (2015) Vol. 51, Iss. 42, pp. 8789-8792
Closed Access | Times Cited: 136

Transition metal-catalyzed C–H bond functionalization in multicomponent reactions: a tool toward molecular diversity
Jie‐Ping Wan, Lu Gan, Yunyun Liu
Organic & Biomolecular Chemistry (2017) Vol. 15, Iss. 43, pp. 9031-9043
Closed Access | Times Cited: 118

Streocontrolled Construction of Six Vicinal Stereogenic Centers on Spiropyrazolones via Organocascade Michael/Michael/1,2-Addition Reactions
Pankaj Chauhan, Suruchi Mahajan, Charles C. J. Loh, et al.
Organic Letters (2014) Vol. 16, Iss. 11, pp. 2954-2957
Open Access | Times Cited: 117

Proline and its Derivatives as Organocatalysts for Multi‐ Component Reactions in Aqueous Media: Synergic Pathways to the Green Synthesis of Heterocycles
B. S. Vachan, Muthu Karuppasamy, Perumal Vinoth, et al.
Advanced Synthesis & Catalysis (2019) Vol. 362, Iss. 1, pp. 87-110
Closed Access | Times Cited: 116

Enantioselective Cascade Michael Addition/Cyclization Reactions of 3‐Nitro‐2H‐Chromenes with 3‐Isothiocyanato Oxindoles: Efficient Synthesis of Functionalized Polycyclic Spirooxindoles
Fen Tan, Liang‐Qiu Lu, Qing‐Qing Yang, et al.
Chemistry - A European Journal (2014) Vol. 20, Iss. 12, pp. 3415-3420
Closed Access | Times Cited: 99

The application of isatin-based multicomponent-reactions in the quest for new bioactive and druglike molecules
Pedro Brandão, Carolina S. Marques, Anthony J. Burke, et al.
European Journal of Medicinal Chemistry (2020) Vol. 211, pp. 113102-113102
Open Access | Times Cited: 97

The Squaramide‐Catalyzed 1,3‐Dipolar Cycloaddition of Nitroalkenes with N‐2,2,2‐Trifluoroethylisatin Ketimines: An Approach for the Synthesis of 5′‐Trifluoromethyl‐spiro[pyrrolidin‐3,2′‐oxindoles]
Quantao Sun, Xiaoyuan Li, Jinhuan Su, et al.
Advanced Synthesis & Catalysis (2015) Vol. 357, Iss. 14-15, pp. 3187-3196
Closed Access | Times Cited: 93

Convenient Synthetic Protocols for Diverse Functionalized Dihydrobenzofuran-Fused Spiro-indanedione-oxindole Scaffolds
Jing Sun, Xueyan Liu, Qiu Sun, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 16, pp. 11562-11580
Closed Access | Times Cited: 23

Combining silver- and organocatalysis: an enantioselective sequential catalytic approach towards pyrano-annulated pyrazoles
Daniel Hack, Pankaj Chauhan, Kristina Deckers, et al.
Chemical Communications (2014) Vol. 51, Iss. 12, pp. 2266-2269
Open Access | Times Cited: 86

Boric acid-catalyzed multi-component reaction for efficient synthesis of 4H-isoxazol-5-ones in aqueous medium
Hamzeh Kiyani, Fatemeh Ghorbani
Research on Chemical Intermediates (2013) Vol. 41, Iss. 5, pp. 2653-2664
Open Access | Times Cited: 85

Recent Advances in Green Synthesis of 3,3′‐Spirooxindoles via Isatin–based One–pot Multicomponent Cascade Reactions in Aqueous Medium
Lijun Yan, Yongchao Wang
ChemistrySelect (2016) Vol. 1, Iss. 21, pp. 6948-6960
Closed Access | Times Cited: 79

Asymmetric synthesis of chiral 3,3-disubstituted oxindoles using isatin as starting material
Ghodsi Mohammadi Ziarani, Razieh Moradi, Negar Lashgari
Tetrahedron Asymmetry (2015) Vol. 26, Iss. 10-11, pp. 517-541
Closed Access | Times Cited: 78

Convenient synthesis of functionalized spiro[indoline-3,2′-pyrrolizines] or spiro[indoline-3,3′-pyrrolidines] via multicomponent reactions
Jing Sun, Liang Chen, Hui Gong, et al.
Organic & Biomolecular Chemistry (2015) Vol. 13, Iss. 21, pp. 5905-5917
Closed Access | Times Cited: 73

Cooperative N-heterocyclic carbene (NHC)–Lewis acid-mediated regioselective umpolung formal [3 + 2] annulations of alkynyl aldehydes with isatins
Yu Zhang, Yingyan Lu, Weifang Tang, et al.
Organic & Biomolecular Chemistry (2014) Vol. 12, Iss. 19, pp. 3009-3015
Closed Access | Times Cited: 72

Recent applications of isatin in the synthesis of organic compounds
Razieh Moradi, Ghodsi Mohammadi Ziarani, Negar Lashgari
ARKIVOC (2017) Vol. 2017, Iss. 1, pp. 148-201
Open Access | Times Cited: 65

Asymmetric synthesis of chiral oxindoles using isatin as starting material
Ghodsi Mohammadi Ziarani, Razieh Moradi, Negar Lashgari
Tetrahedron (2018) Vol. 74, Iss. 13, pp. 1323-1353
Closed Access | Times Cited: 65

Ethyl lactate-involved three-component dehydrogenative reactions: biomass feedstock in diversity-oriented quinoline synthesis
Lu Yang, Jie‐Ping Wan
Green Chemistry (2020) Vol. 22, Iss. 10, pp. 3074-3078
Closed Access | Times Cited: 56

Engaging Isatins in Multicomponent Reactions (MCRs) – Easy Access to Structural Diversity
Pedro Brandão, Carolina S. Marques, Elisabete P. Carreiro, et al.
The Chemical Record (2021) Vol. 21, Iss. 4, pp. 924-1037
Open Access | Times Cited: 43

Page 1 - Next Page

Scroll to top