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:

Deployment of Sulfinimines in Charge-Accelerated Sulfonium Rearrangement Enables a Surrogate Asymmetric Mannich Reaction
Minghao Feng, Ivan Mosiagin, Daniel Kaiser, et al.
Journal of the American Chemical Society (2022) Vol. 144, Iss. 29, pp. 13044-13049
Open Access | Times Cited: 26

Showing 1-25 of 26 citing articles:

Direct enantioselective α-amination of amides guided by DFT prediction of E/Z selectivity in a sulfonium intermediate
Minghao Feng, Anthony J. Fernandes, Ricardo Meyrelles, et al.
Chem (2023) Vol. 9, Iss. 6, pp. 1538-1548
Open Access | Times Cited: 22

Free Amino Group Transfer via α‐Amination of Native Carbonyls
Minghao Feng, Anthony J. Fernandes, Ana Sirvent, et al.
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 28
Open Access | Times Cited: 19

Multicatalysis protocol enables direct and versatile enantioselective reductive transformations of secondary amides
Hang Chen, Zhi-Zhong Wu, Dong-Yang Shao, et al.
Science Advances (2022) Vol. 8, Iss. 47
Open Access | Times Cited: 24

Stereoselective Vinylogous Aza-Pummerer Reaction of β,β-Disubstituted Enesulfinamides
Chong-Lin Zhu, Baozhu Tian, Zonghan Huang, et al.
Organic Letters (2025)
Closed Access

α‐Amination of Carbonyl Compounds by Using Hypervalent Iodine‐Based Aminating Reagents Containing a Transferable (Diarylmethylene)amino Group
Daichi Okumatsu, Kazuki Kawanaka, Shunpei Kainuma, et al.
Chemistry - A European Journal (2023) Vol. 29, Iss. 10
Closed Access | Times Cited: 8

Domino Conjugate Addition-1,4-Aryl Migration for the Synthesis of α,β-Difunctionalized Amides
Haoqi Zhang, Yi Xiao, Miran Lemmerer, et al.
JACS Au (2024) Vol. 4, Iss. 7, pp. 2456-2461
Open Access | Times Cited: 2

Advances in Transition Metal Catalysis and Organocatalysis Approaches towards Asymmetric Synthesis of β-Amino Acid Derivatives
Farrukh Sajjad, Shuyue Zhang, Ming‐Hua Xu
Synthesis (2024)
Closed Access | Times Cited: 2

Sulfonium Rearrangements Enable the Direct Preparation of Sulfenyl Imidinium Salts
Carlos R. Gonçalves, Immo Klose, Simone Placidi, et al.
Angewandte Chemie (2024) Vol. 136, Iss. 9
Open Access | Times Cited: 1

Design, synthesis and antimicrobial activities of novel bis-Mannich bases derived from lawsone
Mohammad Reza Khodabakhshi, Alireza Adl, Abolfazl Olyaei
Research on Chemical Intermediates (2023) Vol. 49, Iss. 11, pp. 4759-4770
Closed Access | Times Cited: 2

Chemoselective α-Trifluoroacetylation of Amides Using Highly Electrophilic Trifluoroacetic Anhydrides and 2,4,6-Collidine
Taiki Morita, Kentaro Makino, Masato Tsuda, et al.
Organic Letters (2023) Vol. 25, Iss. 49, pp. 8901-8905
Closed Access | Times Cited: 2

Synthesis and Functionalization of Tertiary Propargylic Boronic Esters by Alkynyllithium-Mediated 1,2-Metalate Rearrangement of Borylated Cyclopropanes
Tereza Pavlíčková, Yannick Stöckl, Ilan Marek
Organic Letters (2022) Vol. 24, Iss. 48, pp. 8901-8906
Open Access | Times Cited: 4

Sulfonium Rearrangements Enable the Direct Preparation of Sulfenyl Imidinium Salts
Carlos R. Gonçalves, Immo Klose, Simone Placidi, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 9
Open Access

Diastereo‐ and Enantioselective Construction of Stereochemical Arrays Exploiting Non‐Classical Hydrogen Bonding in Enolborates
Matthew Li, Stephan Scheeff, Jiahua Chen, et al.
Chemistry - A European Journal (2024) Vol. 30, Iss. 46
Open Access

Rhodium‐Catalyzed Asymmetric Hydrogenation of Tetrasubstituted α,β‐Unsaturated Amides: Efficient Access to Chiral β‐Amino Amides
Bing Jiao, Fangyuan Wang, Hui Lv
Chinese Journal of Chemistry (2024) Vol. 42, Iss. 21, pp. 2641-2646
Closed Access

Direct Asymmetric Synthesis of α‐Aminoimines from 1,2‐Bis‐N‐Sulfinylimines by Using Allyl Boronic Acids
Susanta Bhunia, Ganesh Karan, Shubham Snehil, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 44
Closed Access

Direct Asymmetric Synthesis of α‐Aminoimines from 1,2‐Bis‐N‐Sulfinylimines by Using Allyl Boronic Acids
Susanta Bhunia, Ganesh Karan, Shubham Snehil, et al.
Angewandte Chemie (2024) Vol. 136, Iss. 44
Closed Access

Hydride Shuttle Catalysis: From Conventional to Inverse Mode
Iakovos Saridakis, Immo Klose, Benjamin T. Jones, et al.
JACS Au (2024) Vol. 4, Iss. 9, pp. 3358-3369
Open Access

Asymmetric Synthesis of β‐Ketoamides by Sulfonium Rearrangement
Vincent Porte, Vinicius R. Nascimento, Ana Sirvent, et al.
Angewandte Chemie International Edition (2024)
Closed Access

Asymmetric Synthesis of β‐Ketoamides by Sulfonium Rearrangement
Vincent Porte, Vinicius R. Nascimento, Ana Sirvent, et al.
Angewandte Chemie (2024)
Closed Access

The Bimolecular and Intramolecular Mannich and Related Reactions
Fujie Tanaka
Elsevier eBooks (2023)
Closed Access | Times Cited: 1

Activation/Cyclization of 2H‐Azirines and 3‐Amino‐2‐fluoropyridines Towards 2‐Aryl‐Pyrido[2,3‐b]pyrazines
Tess Fortier, Audrey Belouin, Frédéric Vuillermet, et al.
European Journal of Organic Chemistry (2024) Vol. 27, Iss. 24
Closed Access

Transfer freier Aminogruppen via α‐Aminierung von Carbonylen
Minghao Feng, Anthony J. Fernandes, Ana Sirvent, et al.
Angewandte Chemie (2023) Vol. 135, Iss. 28
Open Access

Metal-Free α-C(sp3)—H Methylenation of Aryl Ketones to Form γ-Keto Sulfoxides with Dimethyl Sulfoxide
Duoduo Xiao, Jiantao Zhang, Peng Zhou, et al.
Chinese Journal of Organic Chemistry (2023) Vol. 43, Iss. 11, pp. 3900-3900
Open Access

Notizen aus der Chemie
Eva Blasco, Georg Dierkes, Johanna Heine, et al.
Nachrichten aus der Chemie (2022) Vol. 70, Iss. 9, pp. 52-55
Closed Access

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