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:

Asymmetric synthesis of sulfoximines, sulfonimidoyl fluorides and sulfonimidamides enabled by an enantiopure bifunctional S(VI) reagent
Shun Teng, Zachary Shultz, Chuan Shan, et al.
Nature Chemistry (2024) Vol. 16, Iss. 2, pp. 183-192
Open Access | Times Cited: 39

Showing 1-25 of 39 citing articles:

Unlocking Chiral Sulfinimidoyl Electrophiles: Asymmetric Synthesis of Sulfinamides Catalyzed by Anionic Stereogenic-at-Cobalt(III) Complexes
Hua‐Jie Jiang, Fang Wei, Xinran Chen, et al.
Journal of the American Chemical Society (2025)
Closed Access | Times Cited: 2

A reagent to access methyl sulfones
Yaroslav Poplavskyi, Vasyl Ripenko, Sergei Bova, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access | Times Cited: 2

Enantioselective Arylation of Sulfenamides to Access Sulfilimines Enabled by Palladium Catalysis
Yin Yuan, Yidan Han, Zhikun Zhang, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 37
Closed Access | Times Cited: 11

Enantioselective S‐Alkylation of Sulfenamides by Phase‐Transfer Catalysis
Andrew T. Champlin, Na Yeon Kwon, Jonathan A. Ellman
Angewandte Chemie International Edition (2024)
Closed Access | Times Cited: 8

Asymmetric 2,3-Addition of Sulfinylamines with Arylboronic Acids Enabled by Nickel Catalysis
Longlong Xi, Xiaowu Fang, Minyan Wang, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 26, pp. 17587-17594
Closed Access | Times Cited: 7

Rh(II)-Catalyzed Enantioselective S-Alkylation of Sulfenamides with Acceptor–Acceptor Diazo Compounds Enables the Synthesis of Sulfoximines Displaying Diverse Functionality
Shivani Patel, Nathaniel S. Greenwood, Brandon Q. Mercado, et al.
Organic Letters (2024) Vol. 26, Iss. 29, pp. 6295-6300
Closed Access | Times Cited: 6

Synthesis of chiral sulfilimines by organocatalytic enantioselective sulfur alkylation of sulfenamides
Fucheng Wang, Weiming Xiang, Yiting Xie, et al.
Science Advances (2024) Vol. 10, Iss. 37
Open Access | Times Cited: 5

Reductive sulfinylation by nucleophilic chain isomerization of sulfonylpyridinium
Yifan Li, Weigang Zhang, Jeonguk Kweon, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access

Iron-catalysed stereoselective NH transfer enables dynamic kinetic resolution of sulfoxides
Fang-Xu Fan, Hui Xu, Sheng Tang, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access

Assembly of (hetero)aryl sulfilimines via copper-catalyzed enantioselective S-arylation of sulfenamides with (hetero)aryl Iodides
Mingchuang He, Rongxing Zhang, Tongkun Wang, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access

Synthesis of Sulfoximines and Cyclic Sulfoximines
Qingle Zeng, Alex Adonis Nking’wa
(2025), pp. 1-54
Closed Access

Radical Photochemical Difluorosulfoximination of Alkenes and Propellanes
Simone Baldon, Julien Paut, Elsa Anselmi, et al.
Chemical Science (2025)
Open Access

Asymmetric reductive arylation and alkenylation to access S-chirogenic sulfinamides
Xiaowu Fang, Longlong Xi, Minyan Wang, et al.
Nature Communications (2025) Vol. 16, Iss. 1
Open Access

Recent Advances in Asymmetric Synthesis of Chiral-at-Sulfur Sulfoximines
Muhammad Suleman, Tianming Huang, Tao Zhou, et al.
ACS Catalysis (2025), pp. 5511-5530
Closed Access

Poison to promise: The resurgence of organophosphorus fluoride chemistry
William P. Chappell, Natalie Schur, James A. Vogel, et al.
Chem (2024) Vol. 10, Iss. 6, pp. 1644-1654
Closed Access | Times Cited: 3

The Modular Synthesis of Sulfondiimidoyl Fluorides and their Application to Sulfondiimidamide and Sulfondiimine Synthesis
Mingyan Ding, Charles Bell, Michael C. Willis
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 38
Open Access | Times Cited: 3

Catalyst Control over S(IV)-stereogenicity via Carbene-derived Sulfinyl Azolium Intermediates
Benpeng Li, Junyuan Hu, Minghong Liao, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 36, pp. 25350-25360
Closed Access | Times Cited: 3

Computational analysis of modular diazotransfer reactions for the development of predictive reactivity models and diazotransfer reagents
Meng-Meng Zheng, Cai Liu, Tiancheng Ma, et al.
Nature Synthesis (2024)
Closed Access | Times Cited: 3

Sulfur stereochemistry takes centre stage
James A. Bull
Nature Chemistry (2024) Vol. 16, Iss. 2, pp. 152-153
Closed Access | Times Cited: 2

2‐Methylimidazole‐1‐(Ntert‐octyl)sulfonimidoyl Fluoride: A Bench‐Stable Alternative to SOF4 as Precursor to N,O‐Substituted S(VI) Compounds
Natassa Lional, Fedor M. Miloserdov, Han Zuilhof
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 36
Open Access | Times Cited: 2

Strain-release driven reactivity of a chiral SuFEx reagent provides stereocontrolled access to sulfinamides, sulfonimidamides, and sulfoximines
Paresh R. Athawale, Zachary Shultz, Alexandra Saputo, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 2

Cyclic Sulfoximines as Methyl and Perdeuteromethyl Transfer Agents and Their Applications in Photoredox Catalysis
Peng Wu, Gabriel Goujon, Shulei Pan, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 51
Open Access | Times Cited: 2

Enantioselective Synthesis of Chiral Sulfonimidoyl Fluorides Facilitates Stereospecific SuFEx Click Chemistry
He-sen Huang, Yi Yuan, Wei Wang, et al.
Angewandte Chemie International Edition (2024)
Closed Access | Times Cited: 2

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