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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:

Metal-Free Transamidation of Secondary Amides by N–C Cleavage
Md. Mahbubur Rahman, Guangchen Li, Michal Szostak
The Journal of Organic Chemistry (2019) Vol. 84, Iss. 18, pp. 12091-12100
Closed Access | Times Cited: 76

Showing 1-25 of 76 citing articles:

Transition‐Metal‐Free Activation of Amides by N−C Bond Cleavage
Guangchen Li, Michal Szostak
The Chemical Record (2019) Vol. 20, Iss. 7, pp. 649-659
Closed Access | Times Cited: 91

Direct Amidation of Esters by Ball Milling**
William I. Nicholson, Fabien Barreteau, Jamie A. Leitch, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 40, pp. 21868-21874
Closed Access | Times Cited: 65

Highly Chemoselective Transamidation of Unactivated Tertiary Amides by Electrophilic N−C(O) Activation by Amide‐to‐Acyl Iodide Re‐routing
Dongxu Zuo, Qun Wang, Long Liu, et al.
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 24
Open Access | Times Cited: 43

Classes of Amides that Undergo Selective N–C Amide Bond Activation: The Emergence of Ground-State Destabilization
Pengcheng Gao, Md. Mahbubur Rahman, Alfredo Zamalloa, et al.
The Journal of Organic Chemistry (2022) Vol. 88, Iss. 19, pp. 13371-13391
Closed Access | Times Cited: 41

Non-Classical Amide Bond Formation: Transamidation and Amidation of Activated Amides and Esters by Selective N–C/O–C Cleavage
Michal Szostak, Guangchen Li
Synthesis (2020) Vol. 52, Iss. 18, pp. 2579-2599
Closed Access | Times Cited: 67

Transamidation for the Synthesis of Primary Amides at Room Temperature
Jiajia Chen, Yuanzhi Xia, Sunwoo Lee
Organic Letters (2020) Vol. 22, Iss. 9, pp. 3504-3508
Closed Access | Times Cited: 62

Palladium-Catalyzed Amide N–C Hiyama Cross-Coupling: Synthesis of Ketones
Muhammad Aliyu Idris, Sunwoo Lee
Organic Letters (2020) Vol. 22, Iss. 23, pp. 9190-9195
Closed Access | Times Cited: 42

A practical and sustainable protocol for direct amidation of unactivated esters under transition-metal-free and solvent-free conditions
Rui Zhang, Wei‐Zhong Yao, Liang Qian, et al.
Green Chemistry (2021) Vol. 23, Iss. 11, pp. 3972-3982
Open Access | Times Cited: 41

Tungsten-Catalyzed Transamidation of Tertiary Alkyl Amides
Fang‐Fang Feng, Xuan‐Yu Liu, Chi Wai Cheung, et al.
ACS Catalysis (2021) Vol. 11, Iss. 12, pp. 7070-7079
Closed Access | Times Cited: 35

Copper-Catalyzed Transamidation of Unactivated Secondary Amides via C–H and C–N Bond Simultaneous Activations
Cong Lv, Ruisheng Zhao, Xiuying Wang, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 4, pp. 2140-2157
Closed Access | Times Cited: 16

B2(OH)4-Mediated Reductive Transamidation of N-Acyl Benzotriazoles with Nitro Compounds En Route to Aqueous Amide Synthesis
Jin Bai, Shangzhang Li, Riqian Zhu, et al.
The Journal of Organic Chemistry (2023) Vol. 88, Iss. 6, pp. 3714-3723
Closed Access | Times Cited: 15

Direct Amidation of Carboxylic Acids with Nitroarenes
Shao-Peng Wang, Chi Wai Cheung, Jun‐An Ma
The Journal of Organic Chemistry (2019) Vol. 84, Iss. 21, pp. 13922-13934
Closed Access | Times Cited: 41

Ultrafast amidation of esters using lithium amides under aerobic ambient temperature conditions in sustainable solvents
Michael Fairley, Leonie J. Bole, Florian F. Mulks, et al.
Chemical Science (2020) Vol. 11, Iss. 25, pp. 6500-6509
Open Access | Times Cited: 38

Transamidation of thioamides with nucleophilic amines: thioamide N–C(S) activation by ground-state-destabilization
Jin Zhang, Hui Zhao, Guangchen Li, et al.
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 30, pp. 5981-5988
Closed Access | Times Cited: 20

C–C Bond Cleavage-Induced C- to N-Acyl Transfer for Synthesis of Amides
Su Eun Lee, Youngsoo Kim, Yong Ho Lee, et al.
Organic Letters (2024) Vol. 26, Iss. 17, pp. 3646-3651
Closed Access | Times Cited: 4

Transamidation via C–N bond cleavage of amides and tertiary amines
Muhammad Aliyu Idris, Sunwoo Lee
Organic Chemistry Frontiers (2020) Vol. 7, Iss. 18, pp. 2737-2743
Closed Access | Times Cited: 27

Visible-Light Photoredox-Catalyzed Amidation of Benzylic Alcohols
Silvia Gaspa, Andrea Farina, Mariella Tilocca, et al.
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 18, pp. 11679-11687
Open Access | Times Cited: 26

Green-Solvent Selection for Acyl Buchwald–Hartwig Cross-Coupling of Amides (Transamidation)
Peng Lei, Yi‐Bo Wang, Yali Mu, et al.
ACS Sustainable Chemistry & Engineering (2021) Vol. 9, Iss. 44, pp. 14937-14945
Closed Access | Times Cited: 23

Nickel-Catalyzed Reductive Cross-Coupling of N-Acyl and N-Sulfonyl Benzotriazoles with Diverse Nitro Compounds: Rapid Access to Amides and Sulfonamides
Erdong Qu, Shangzhang Li, Jin Bai, et al.
Organic Letters (2021) Vol. 24, Iss. 1, pp. 58-63
Closed Access | Times Cited: 22

Solvent- and additive-free oxidative amidation of aldehydes using a recyclable oxoammonium salt
Arturo León Sandoval, Katrina E. Doherty, Geoffrey P. Wadey, et al.
Organic & Biomolecular Chemistry (2022) Vol. 20, Iss. 11, pp. 2249-2254
Closed Access | Times Cited: 16

Amide Synthesis by Transamidation of Primary Carboxamides
Sylvain Laclef, Maria Kolympadi, Dean Marković
Synthesis (2020) Vol. 52, Iss. 21, pp. 3231-3242
Closed Access | Times Cited: 22

Diversification of α-ketoamides via transamidation reactions with alkyl and benzyl amines at room temperature
Shweta Singh, Popuri Sureshbabu, Qazi Mohammad Junaid, et al.
Organic & Biomolecular Chemistry (2021) Vol. 19, Iss. 33, pp. 7134-7140
Closed Access | Times Cited: 20

A CO2-Catalyzed Transamidation Reaction
Yang Yang, Jian Liu, Fadhil S. Kamounah, et al.
The Journal of Organic Chemistry (2021) Vol. 86, Iss. 23, pp. 16867-16881
Closed Access | Times Cited: 19

Nickel/briphos-catalyzed transamidation of unactivated tertiary amides
Dahyeon Yang, Taeil Shin, Hyunwoo Kim, et al.
Organic & Biomolecular Chemistry (2020) Vol. 18, Iss. 31, pp. 6053-6057
Closed Access | Times Cited: 20

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