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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!

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Requested Article:

Asymmetric Synthesis of Spirocyclic Oxindole‐Fused Tetrahydrothiophenes via N,N′‐Dioxide–Nickel(II) Catalyzed Domino Reaction of 1,4‐Dithiane‐2,5‐diol with 3‐Alkenyloxindoles
Pengfei Zhou, Yunfei Cai, Lili Lin, et al.
Advanced Synthesis & Catalysis (2015) Vol. 357, Iss. 4, pp. 695-700
Closed Access | Times Cited: 51

Showing 1-25 of 51 citing articles:

Catalytic asymmetric synthesis of spirooxindoles: recent developments
Guang‐Jian Mei, Feng Shi
Chemical Communications (2018) Vol. 54, Iss. 50, pp. 6607-6621
Closed Access | Times Cited: 400

Asymmetric Cycloaddition and Cyclization Reactions Catalyzed by Chiral N,N′-Dioxide–Metal Complexes
Xiaohua Liu, Haifeng Zheng, Yong Xia, et al.
Accounts of Chemical Research (2017) Vol. 50, Iss. 10, pp. 2621-2631
Closed Access | Times Cited: 398

New development in the enantioselective synthesis of spiro compounds
Aishun Ding, Marta Meazza, Hao Guo, et al.
Chemical Society Reviews (2018) Vol. 47, Iss. 15, pp. 5946-5996
Open Access | Times Cited: 362

Recent Advances in Metal-Catalyzed Asymmetric 1,4-Conjugate Addition (ACA) of Nonorganometallic Nucleophiles
Ke Zheng, Xiaohua Liu, Xiaoming Feng
Chemical Reviews (2018) Vol. 118, Iss. 16, pp. 7586-7656
Closed Access | Times Cited: 293

Catalytic Enantioselective Construction of Spiro Quaternary Carbon Stereocenters
Pengwei Xu, Jin‐Sheng Yu, Chen Chen, et al.
ACS Catalysis (2019) Vol. 9, Iss. 3, pp. 1820-1882
Closed Access | Times Cited: 273

Catalytic enantioselective aldol reactions
Yasuhiro Yamashita, Tomohiro Yasukawa, Woo‐Jin Yoo, et al.
Chemical Society Reviews (2018) Vol. 47, Iss. 12, pp. 4388-4480
Closed Access | Times Cited: 269

Recent Developments in Enantioselective Metal‐Catalyzed Domino Reactions
Hélène Pellissier
Advanced Synthesis & Catalysis (2016) Vol. 358, Iss. 14, pp. 2194-2259
Open Access | Times Cited: 110

Metal-catalyzed C–S bond formation using sulfur surrogates
Nallappan Sundaravelu, Subramani Sangeetha, Govindasamy Sekar
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 7, pp. 1459-1482
Closed Access | Times Cited: 89

Recent Advances of α‐Isothiocyanato Compounds in the Catalytic Asymmetric Reaction
Wen‐Yong Han, Jian‐Qiang Zhao, Jian Zuo, et al.
Advanced Synthesis & Catalysis (2015) Vol. 357, Iss. 14-15, pp. 3007-3031
Closed Access | Times Cited: 86

The asymmetric synthesis of polycyclic 3-spirooxindole alkaloids via the cascade reaction of 2-isocyanoethylindoles
Xiaohu Zhao, Xiaohua Liu, Qian Xiong, et al.
Chemical Communications (2015) Vol. 51, Iss. 89, pp. 16076-16079
Closed Access | Times Cited: 74

Stereoselective Domino Reactions in the Synthesis of Spiro Compounds
Maurizio Benaglia, Sandro J. Greco, Regina Westphal, et al.
Synthesis (2022) Vol. 54, Iss. 13, pp. 2927-2975
Open Access | Times Cited: 29

The enantioselective construction of chiral spirooxindole-based 4-thiazolidinone via asymmetric catalytic formal [3+2] annulation using a bifunctional catalyst
Ping Cheng, Wengang Guo, Ping Chen, et al.
Chemical Communications (2016) Vol. 52, Iss. 16, pp. 3418-3421
Closed Access | Times Cited: 47

Asymmetric Synthesis of 3,3′-Tetrahydrofuryl Spirooxindoles via Palladium-Catalyzed [3+2] Cycloadditions of Methyleneindolinones with Vinylethylene Carbonates
Junwei Wang, Lei Zhao, Quanjin Rong, et al.
Organic Letters (2020) Vol. 22, Iss. 15, pp. 5833-5838
Closed Access | Times Cited: 40

Rh(II)/Chiral Phosphoric Acid-Cocatalyzed Enantioselective Synthesis of Spirooxindole-Fused Thiaindans
Guolan Xiao, Tiantian Chen, Chaoqun Ma, et al.
Organic Letters (2018) Vol. 20, Iss. 15, pp. 4531-4535
Closed Access | Times Cited: 46

1,4‐Dithiane‐2,5‐diol: An Attractive Platform for the Synthesis of Sulfur‐Containing Functionalized Heterocycles
Francesco Zamberlan, Anna Fantinati, Claudio Trapella
European Journal of Organic Chemistry (2018) Vol. 2018, Iss. 25, pp. 3248-3264
Open Access | Times Cited: 38

Synthesis of Spirocyclic Oxindole Dihydrothiophenes by DBU-Catalyzed [3 + 2] Annulation of Morita–Baylis–Hillman Carbonates with Isothiocyanates
Yuan‐Yuan Zhao, Shuai Zhao, Ji‐Kang Xie, et al.
The Journal of Organic Chemistry (2016) Vol. 81, Iss. 21, pp. 10532-10537
Closed Access | Times Cited: 33

Synthesis of spiro-tetrahydrothiopyran-oxindoles by Michael–aldol cascade reactions: discovery of potential P53-MDM2 inhibitors with good antitumor activity
Shengzheng Wang, Shuqiang Chen, Zhongjie Guo, et al.
Organic & Biomolecular Chemistry (2017) Vol. 16, Iss. 4, pp. 625-634
Closed Access | Times Cited: 31

Organocatalytic Asymmetric Synthesis of Spiro‐Tetrahydrothiophene Oxindoles Bearing Four Contiguous Stereocenters by One‐Pot Michael–Henry‐Cascade–Rearrangement Reactions
Shengzheng Wang, Zhongjie Guo, Shuqiang Chen, et al.
Chemistry - A European Journal (2017) Vol. 24, Iss. 1, pp. 62-66
Closed Access | Times Cited: 28

Cascade reactions as efficient and universal tools for construction and modification of 6-, 5-, 4- and 3-membered sulfur heterocycles of biological relevance
Piotr Przybylski, Katarzyna Pyta-Klich, Krystian Pyta, et al.
Tetrahedron (2018) Vol. 74, Iss. 44, pp. 6335-6365
Closed Access | Times Cited: 26

Asymmetric [3+2] annulations of 1,4-di-thiane-2,5-diol and oxindole ketimines
Boxu Feng, Jin‐Dong Yang, Jiuyuan Li, et al.
Tetrahedron Letters (2016) Vol. 57, Iss. 31, pp. 3457-3461
Closed Access | Times Cited: 25

Magnesium‐Catalyzed Asymmetric Thia‐Michael Addition to α,β‐Unsaturated Ketones
Joanna A. Jaszczewska‐Adamczak, Paulina Baczewska, Robert Bujok, et al.
Advanced Synthesis & Catalysis (2024) Vol. 366, Iss. 6, pp. 1412-1421
Closed Access | Times Cited: 2

Design, synthesis and biological evaluation of novel antitumor spirodihydrothiopyran-oxindole derivatives
Wei Liu, Shuqiang Chen, Fan Zhang, et al.
Bioorganic & Medicinal Chemistry Letters (2019) Vol. 29, Iss. 13, pp. 1636-1642
Closed Access | Times Cited: 20

The Molecular Diversity Scope of Oxindole Derivatives in Organic Synthesis
Ghodsi Mohammadi Ziarani, Fatemeh Javadi, Fatemeh Mohajer
Current Organic Chemistry (2021) Vol. 25, Iss. 7, pp. 779-818
Closed Access | Times Cited: 16

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