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:

Organocatalytic Chlorination of Alcohols by P(III)/P(V) Redox Cycling
Lars Longwitz, Stefan Jopp, Thomas Werner
The Journal of Organic Chemistry (2019) Vol. 84, Iss. 12, pp. 7863-7870
Closed Access | Times Cited: 26

Showing 1-25 of 26 citing articles:

Phosphorus-Based Catalysis
Changmin Xie, Andrew J. Smaligo, Xian-Rong Song, et al.
ACS Central Science (2021) Vol. 7, Iss. 4, pp. 536-558
Open Access | Times Cited: 233

Main Group Redox Catalysis of Organopnictogens: Vertical Periodic Trends and Emerging Opportunities in Group 15
Jeffrey M. Lipshultz, Gen Li, Alexander T. Radosevich
Journal of the American Chemical Society (2021) Vol. 143, Iss. 4, pp. 1699-1721
Open Access | Times Cited: 216

Phosphetane Oxides as Redox Cycling Catalysts in the Catalytic Wittig Reaction at Room Temperature
Lars Longwitz, Anke Spannenberg, Thomas Werner
ACS Catalysis (2019) Vol. 9, Iss. 10, pp. 9237-9244
Closed Access | Times Cited: 46

Lewis Base Catalysis Promoted Nucleophilic Substitutions – Recent Advances and Future Directions
Peter H. Huy
European Journal of Organic Chemistry (2019) Vol. 2020, Iss. 1, pp. 10-27
Open Access | Times Cited: 45

Reduction of Activated Alkenes by P III /P V Redox Cycling Catalysis
Lars Longwitz, Thomas Werner
Angewandte Chemie International Edition (2019) Vol. 59, Iss. 7, pp. 2760-2763
Open Access | Times Cited: 41

Development of a More Sustainable Appel Reaction
Andrew Jordan, Ross M. Denton, Helen F. Sneddon
ACS Sustainable Chemistry & Engineering (2020) Vol. 8, Iss. 5, pp. 2300-2309
Closed Access | Times Cited: 34

Synthesis, biocompatibility, and antimicrobial properties of glucose-based ionic liquids
Stefan Jopp, Tabea Fleischhammer, Antonina Lavrentieva, et al.
RSC Sustainability (2023) Vol. 1, Iss. 7, pp. 1751-1764
Open Access | Times Cited: 11

Organophosphorus catalytic reaction based on reduction of phosphine oxide
Mengyu Pei, Anqi Tian, Qing‐Qing Yang, et al.
Green Synthesis and Catalysis (2022) Vol. 4, Iss. 2, pp. 135-149
Open Access | Times Cited: 18

Organophosphorus-catalyzed relay oxidation of H-Bpin: electrophilic C–H borylation of heteroarenes
Jeffrey M. Lipshultz, Yue Fu, Peng Liu, et al.
Chemical Science (2020) Vol. 12, Iss. 3, pp. 1031-1037
Open Access | Times Cited: 26

Organocatalytic Deoxyhalogenation of Alcohols with Inorganic Halides
Weijin Wang, Hongye Wang, Rongheng Dai, et al.
ACS Catalysis (2023) Vol. 13, Iss. 13, pp. 9033-9040
Closed Access | Times Cited: 8

Thiourea-Mediated Halogenation of Alcohols
Amar R. Mohite, Ravindra S. Phatake, P. K. Dubey, et al.
The Journal of Organic Chemistry (2020) Vol. 85, Iss. 20, pp. 12901-12911
Closed Access | Times Cited: 20

Catalytic Vilsmeier–Haack Reactions for C1-Deuterated Formylation of Indoles
Jing Xue, Yushan Zhang, Zhen Huan, et al.
The Journal of Organic Chemistry (2022) Vol. 87, Iss. 22, pp. 15539-15546
Closed Access | Times Cited: 11

Advances in Organophosphorus Redox Catalysis
Wei Cai, You Huang
Chinese Journal of Organic Chemistry (2021) Vol. 41, Iss. 10, pp. 3903-3903
Open Access | Times Cited: 15

Poly(methylhydrosiloxane) as a reductant in the catalytic base-free Wittig reaction
Jan Tönjes, Lars Longwitz, Thomas Werner
Green Chemistry (2021) Vol. 23, Iss. 13, pp. 4852-4857
Closed Access | Times Cited: 13

Organocatalytic Stereospecific Appel Reaction
Jan Tönjes, Lukas Kell, Thomas Werner
Organic Letters (2023) Vol. 25, Iss. 51, pp. 9114-9118
Closed Access | Times Cited: 5

Synthesis of glycosyl chlorides using catalytic Appel conditions
Imlirenla Pongener, Kirill Nikitin, Eoghan M. McGarrigle
Organic & Biomolecular Chemistry (2019) Vol. 17, Iss. 32, pp. 7531-7535
Closed Access | Times Cited: 12

An environmentally benign and high-rate Appel type reaction
Nicolas Mattias Del Rio Fuenzalida, Eirin Alme, Frida Johanne Lundevall, et al.
Reaction Chemistry & Engineering (2022) Vol. 7, Iss. 7, pp. 1650-1659
Open Access | Times Cited: 7

Reduction of Activated Alkenes by PIII/PV Redox Cycling Catalysis
Lars Longwitz, Thomas Werner
Angewandte Chemie (2019) Vol. 132, Iss. 7, pp. 2782-2785
Closed Access | Times Cited: 10

Phosphine‐Catalyzed Synthesis of Chiral N‐Heterocycles through (Asymmetric) P(III)/P(V) Redox Cycling
Charlotte Lorton, Nidal Saleh, Arnaud Voituriez
European Journal of Organic Chemistry (2021) Vol. 2021, Iss. 22, pp. 3340-3344
Open Access | Times Cited: 8

A Synthesis of Furan-2-iminophosphoranes under Appel-Type Reaction Conditions
Issa Yavari, Hamed Saffarian, Omid Khaledian
Synlett (2022) Vol. 34, Iss. 02, pp. 133-136
Closed Access | Times Cited: 3

Convergent Synthesis of Polysubstituted Furans via Catalytic Phosphine Mediated Multicomponent Reactions
Fan Xia, Rongshun Chen, Jie Han, et al.
Molecules (2019) Vol. 24, Iss. 24, pp. 4595-4595
Open Access | Times Cited: 2

Selective monochlorination of unsymmetrical vicinal diols with chlorinated iminium chlorides
Liqun Yang, Xiaotong Li, Yu Wang, et al.
Tetrahedron (2020) Vol. 76, Iss. 17, pp. 131114-131114
Closed Access | Times Cited: 2

Miscellaneous Reactions
Surya K. De
(2020), pp. 161-291
Closed Access

N-bromosuccinimide promoted synthesis of β-amino bromides under Appel reaction condition
C. Srinivasulu, Nanda Hampasagarada Alavandimat, Vathsala Umesha, et al.
Synthetic Communications (2021) Vol. 51, Iss. 19, pp. 2975-2983
Closed Access

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