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:

Tunable and Cooperative Catalysis for Enantioselective Pictet‐Spengler Reaction with Varied Nitrogen‐Containing Heterocyclic Carboxaldehydes
Yuk‐Cheung Chan, Marcus H. Sak, Scott A. Frank, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 46, pp. 24573-24581
Open Access | Times Cited: 23

Showing 23 citing articles:

Screening for generality in asymmetric catalysis
Corin Wagen, Spencer E. McMinn, Eugene E. Kwan, et al.
Nature (2022) Vol. 610, Iss. 7933, pp. 680-686
Open Access | Times Cited: 66

Enantioselective Pictet–Spengler Reaction of Acyclic α-Ketoesters Using Chiral Imidazoline-Phosphoric Acid Catalysts
Shuichi Nakamura, Yoichiro Matsuda, Tsunayoshi Takehara, et al.
Organic Letters (2022) Vol. 24, Iss. 4, pp. 1072-1076
Closed Access | Times Cited: 38

Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst
Rémi Andres, Qian Wang, Jieping Zhu
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 19
Open Access | Times Cited: 30

A genetic optimization strategy with generality in asymmetric organocatalysis as a primary target
Simone Gallarati, Puck van Gerwen, Rubén Laplaza, et al.
Chemical Science (2024) Vol. 15, Iss. 10, pp. 3640-3660
Open Access | Times Cited: 7

Polymer‐Supported Phosphoric‐Acid Catalysed Enantioselective Pictet‐Spengler Cyclisation for the Synthesis of Quaternary Tryptolines in Batch/Continuous Flow
Moreshwar B. Chaudhari, Prachi Gupta, Patricia Llanes, et al.
Advanced Synthesis & Catalysis (2023) Vol. 365, Iss. 4, pp. 527-534
Closed Access | Times Cited: 14

Organocatalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoesters: Development and Application to the Total Synthesis of (+)‐Alstratine A
Rémi Andres, Fenggang Sun, Qian Wang, et al.
Angewandte Chemie International Edition (2022) Vol. 62, Iss. 1
Closed Access | Times Cited: 21

Organocatalyzed Asymmetric Pictet‐Spengler Reactions
Anup Biswas
ChemistrySelect (2023) Vol. 8, Iss. 3
Closed Access | Times Cited: 12

Catalytic enantioselective nitrone cycloadditions enabling collective syntheses of indole alkaloids
Xiaochen Tian, Tengfei Xuan, Jing-Kun Gao, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 4

Enantioselective intramolecular Pictet–Spengler type annulation of indole-linked 3-methyleneisoindolin-1-ones
Min Liu, Wenzhe Li, Min Huang, et al.
New Journal of Chemistry (2022) Vol. 46, Iss. 20, pp. 9582-9586
Closed Access | Times Cited: 11

Rational Design and Stereodivergent Construction of Enantioenriched Tetrahydro-β-Carbolines Containing Multistereogenic Centers
Taotao Chen, Qi Xiong, Hui Xu, et al.
Journal of the American Chemical Society (2024) Vol. 146, Iss. 43, pp. 29928-29942
Closed Access | Times Cited: 2

Pentafluorophenol (C6F5OH) Catalyzed Pictet‐Spengler Reaction: A Facile and Metal‐Free Approach Towards Tetrahydro‐β‐Carbolines
Rina Mahato, Chinmoy Kumar Hazra
Chemistry - A European Journal (2023) Vol. 29, Iss. 27
Closed Access | Times Cited: 6

Screening for Generality in Asymmetric Catalysis
Corin Wagen, Spencer E. McMinn, Eugene E. Kwan, et al.
(2022)
Open Access | Times Cited: 9

Catalytic C–C Bond Forming Reaction to Imines
Branislav Kokić, Ana Andrijević, Igor Opsenica
Elsevier eBooks (2024)
Closed Access | Times Cited: 1

Construction of Diverse N-Heterocycles by Formal (3 + 3) Cycloaddition of Naphthol/Thionaphthol/Naphthylamine and 1,3,5-Triazinanes
Xiang Liu, Yuhan Wang, Huitao Zheng, et al.
The Journal of Organic Chemistry (2022) Vol. 88, Iss. 1, pp. 75-85
Closed Access | Times Cited: 5

Design, Synthesis and Antioxidant Activity of Tetrahydro-β-carbolines
Xiaoyu Zhang, Xinyan Li, Bing Cui, et al.
Chinese Journal of Organic Chemistry (2023) Vol. 43, Iss. 8, pp. 2885-2885
Open Access | Times Cited: 2

A Genetic Optimization Strategy with Generality in Asymmetric Organocatalysis as Primary Target
Simone Gallarati, Puck van Gerwen, Rubén Laplaza, et al.
(2023)
Open Access | Times Cited: 2

Catalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoamides Catalyzed by a Single H‐Bond Donor Organocatalyst
Rémi Andres, Qian Wang, Jieping Zhu
Angewandte Chemie (2022) Vol. 134, Iss. 19
Open Access | Times Cited: 4

The crystal structure of (1S,3R)-1-(4-isopropylphenyl)-3-(methoxycarbonyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indol-2-iumchloride monohydrate, C22H27ClN2O3
Jingxiao Zhang, Miao Gu, Xinyu Bai
Zeitschrift für Kristallographie - New Crystal Structures (2022) Vol. 237, Iss. 4, pp. 619-621
Open Access | Times Cited: 4

N-Fluorenyltryptamines as a Useful Platform for Catalytic Enantio­selective Pictet–Spengler Reactions
Alafate Adili, Aniket V. Sole, Daniel Seidel, et al.
Synthesis (2022) Vol. 55, Iss. 11, pp. 1724-1735
Closed Access | Times Cited: 4

Enantioselective Pictet–Spengler Reactions
Daniel Seidel
Organic reactions (2024), pp. 507-611
Closed Access

Asymmetric Organocatalyzed Synthesis of α‐Aminophosphinates via Thiourea Anion‐Binding Catalysis
Cáoimhe J. Niland, Joseph J. Ruddy, Martin P. O'Fearraigh, et al.
European Journal of Organic Chemistry (2023) Vol. 27, Iss. 11
Open Access | Times Cited: 1

Organocatalytic Enantioselective Pictet–Spengler Reaction of α‐Ketoesters: Development and Application to the Total Synthesis of (+)‐Alstratine A
Rémi Andres, Fenggang Sun, Qian Wang, et al.
Angewandte Chemie (2022) Vol. 135, Iss. 1
Closed Access | Times Cited: 2

Crystal structure of methyl 2-(2-chloroacetyl)-1-(4-(methoxycarbonyl)phenyl)-2,3,4,9-tetrahydro-1H-pyrido[3,4-b] indole-3-carboxylate, C23H21ClN2O5
Xiaona Xu, Zhoujing Zhu, Bin Liu
Zeitschrift für Kristallographie - New Crystal Structures (2023) Vol. 238, Iss. 2, pp. 355-357
Open Access

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