Open Access Helper

OpenAlex Citation Counts

OpenAlex Citations Logo

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:

Rationalizing the diverse reactivity of [1.1.1]propellane through σ–π-delocalization
Alistair J. Sterling, Alexander B. Dürr, Russell C. Smith, et al.
Chemical Science (2020) Vol. 11, Iss. 19, pp. 4895-4903
Open Access | Times Cited: 48

Showing 1-25 of 48 citing articles:

Visible‐Light‐Induced 1,3‐Aminopyridylation of [1.1.1]Propellane with N‐Aminopyridinium Salts
Sanghoon Shin, Seojin Lee, Wonjun Choi, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 14, pp. 7873-7879
Closed Access | Times Cited: 141
Synthesis of meta-substituted arene bioisosteres from [3.1.1]propellane
Nils Frank, Jeremy Nugent, Bethany R. Shire, et al.
Nature (2022) Vol. 611, Iss. 7937, pp. 721-726
Closed Access | Times Cited: 135
Strain-Release Photocatalysis
Peter Bellotti, Frank Glorius
Journal of the American Chemical Society (2023) Vol. 145, Iss. 38, pp. 20716-20732
Closed Access | Times Cited: 114
Conquering the Synthesis and Functionalization of Bicyclo[1.1.1]pentanes
Bethany R. Shire, Edward A. Anderson
JACS Au (2023) Vol. 3, Iss. 6, pp. 1539-1553
Open Access | Times Cited: 73
Three-dimensional saturated C(sp3)-rich bioisosteres for benzene
Jet Tsien, Chao Hu, Rohan R. Merchant, et al.
Nature Reviews Chemistry (2024) Vol. 8, Iss. 8, pp. 605-627
Closed Access | Times Cited: 31
Bridge Functionalisation of Bicyclo[1.1.1]pentane Derivatives
Joseph M. Anderson, Nicholas D. Measom, John A. Murphy, et al.
Angewandte Chemie International Edition (2021) Vol. 60, Iss. 47, pp. 24754-24769
Open Access | Times Cited: 90
Synthesis of All‐Carbon Disubstituted Bicyclo[1.1.1]pentanes by Iron‐Catalyzed Kumada Cross‐Coupling
Jeremy Nugent, Bethany R. Shire, Dimitri F. J. Caputo, et al.
Angewandte Chemie International Edition (2020) Vol. 59, Iss. 29, pp. 11866-11870
Open Access | Times Cited: 70
Direct catalytic asymmetric synthesis of α-chiral bicyclo[1.1.1]pentanes
Marie L. J. Wong, Alistair J. Sterling, James J. Mousseau, et al.
Nature Communications (2021) Vol. 12, Iss. 1
Open Access | Times Cited: 56
Strain‐Release Pentafluorosulfanylation and Tetrafluoro(aryl)sulfanylation of [1.1.1]Propellane: Reactivity and Structural Insight**
Yannick Kraemer, Clément Ghiazza, Abbey N. Ragan, et al.
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 48
Open Access | Times Cited: 48
On-DNA Hydroalkylation to Introduce Diverse Bicyclo[1.1.1]pentanes and Abundant Alkyls via Halogen Atom Transfer
Expédite Yen‐Pon, Longbo Li, Guillaume Levitre, et al.
Journal of the American Chemical Society (2022) Vol. 144, Iss. 27, pp. 12184-12191
Open Access | Times Cited: 39
Synthesis of 1-perfluoroalkyl-3-heteroaryl bicyclo[1.1.1]pentanes via visible light-induced and metal-free perfluoroalkylation of [1.1.1]propellane
Boan Yan, Gongcheng Xu, Hang Han, et al.
Green Chemistry (2023) Vol. 25, Iss. 5, pp. 1948-1954
Closed Access | Times Cited: 35
Highly Regioselective Addition of Allylic Zinc Halides and Various Zinc Enolates to [1.1.1]Propellane
Kuno Schwärzer, Hendrik Zipse, Konstantin Karaghiosoff, et al.
Angewandte Chemie International Edition (2020) Vol. 59, Iss. 45, pp. 20235-20241
Open Access | Times Cited: 66
Electrophilic Activation of [1.1.1]Propellane for the Synthesis of Nitrogen‐Substituted Bicyclo[1.1.1]pentanes
Sarah Livesley, Alistair J. Sterling, Craig M. Robertson, et al.
Angewandte Chemie International Edition (2021) Vol. 61, Iss. 2
Open Access | Times Cited: 40
Nickel-mediated alkyl-, acyl-, and sulfonylcyanation of [1.1.1]propellane
Weizhe Dong, Sebastian Keeß, Gary A. Molander
Chem Catalysis (2023) Vol. 3, Iss. 5, pp. 100608-100608
Open Access | Times Cited: 17
Decoration on Cubane with an Awareness of Chirality: Development of Substituted Cubane Syntheses
Seijiro Matsubara, Hiyori Takebe
Synthesis (2023) Vol. 56, Iss. 01, pp. 16-28
Closed Access | Times Cited: 17
Beyond Strain Release: Delocalization-Enabled Organic Reactivity
Alistair J. Sterling, Russell C. Smith, Edward A. Anderson, et al.
The Journal of Organic Chemistry (2024) Vol. 89, Iss. 14, pp. 9979-9989
Open Access | Times Cited: 6
Better Together: Catalyzing Innovation in Organic Synthesis via Academic-Industrial Consortia
Jesús Alcázar, Edward A. Anderson, Huw M. L. Davies, et al.
Organic Letters (2024) Vol. 26, Iss. 14, pp. 2677-2681
Open Access | Times Cited: 5
Controllable Diverse Construction of gem-Difluoroallylated Bicyclo[1.1.1]pentanes and Cyclobutanes from [1.1.1]Propellane via Copper Catalysis
Xiao‐Tian Feng, Qiao‐Qiao Min, Xin Zeng, et al.
ACS Catalysis (2024) Vol. 14, Iss. 8, pp. 5879-5887
Closed Access | Times Cited: 5
Synthesis of bicyclo[3.1.1]heptanes, meta-substituted arene isosteres, from [3.1.1]propellane
Bhaskar Paul, Ayan Dasgupta, Nils Frank, et al.
Nature Protocols (2025)
Closed Access
Radical Multicomponent Alkyl Alkynylation of Propellane via Synergistic Photoredox and Copper Catalysis
Jie Shi, Qiao-Lin Xu, Yu‐Qing Ni, et al.
Organic Letters (2022) Vol. 24, Iss. 25, pp. 4609-4614
Closed Access | Times Cited: 22
α-Amino Bicycloalkylation through Organophotoredox Catalysis
Jeremy Nugent, Adrián López‐Francés, Alistair J. Sterling, et al.
Chemical Science (2024) Vol. 15, Iss. 28, pp. 10918-10925
Open Access | Times Cited: 4
Reversing Benzene/Cyclohexane Selectivity through Varying Supramolecular Interactions Using Aliphatic, Isoreticular MOFs
Lauren K. Macreadie, Omid T. Qazvini, Ravichandar Babarao
ACS Applied Materials & Interfaces (2021) Vol. 13, Iss. 26, pp. 30885-30890
Closed Access | Times Cited: 31
Synthetic routes to bicyclo[1.1.1]pentylamines: booming toolkits for drug design
Zhiyou Yu, Lei Shi
Organic Chemistry Frontiers (2022) Vol. 9, Iss. 13, pp. 3591-3597
Closed Access | Times Cited: 19
Synthesis of Imidized Cyclobutene Derivatives by Strain Release of [1.1.1]Propellane
Xiaofan Du, Di Xu, Gongcheng Xu, et al.
Organic Letters (2022) Vol. 24, Iss. 40, pp. 7323-7327
Closed Access | Times Cited: 17
Radical Acylation of [1.1.1]Propellane with Aldehydes: Synthesis of Bicyclo[1.1.1]pentane Ketones
Qing Li, Lin Li, Qiaoling Xu, et al.
Organic Letters (2022) Vol. 24, Iss. 23, pp. 4292-4297
Closed Access | Times Cited: 15
Page 1 - Next Page

Scroll to top