
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:
Synthesis of 1,3-disubstituted bicyclo[1.1.0]butanes via directed bridgehead functionalization
Ryan E. McNamee, Marius M. Haugland, Jeremy Nugent, et al.
Chemical Science (2021) Vol. 12, Iss. 21, pp. 7480-7485
Open Access | Times Cited: 45
Ryan E. McNamee, Marius M. Haugland, Jeremy Nugent, et al.
Chemical Science (2021) Vol. 12, Iss. 21, pp. 7480-7485
Open Access | Times Cited: 45
Showing 1-25 of 45 citing articles:
Bicyclobutanes: from curiosities to versatile reagents and covalent warheads
Christopher B. Kelly, John A. Milligan, Leon J. Tilley, et al.
Chemical Science (2022) Vol. 13, Iss. 40, pp. 11721-11737
Open Access | Times Cited: 153
Christopher B. Kelly, John A. Milligan, Leon J. Tilley, et al.
Chemical Science (2022) Vol. 13, Iss. 40, pp. 11721-11737
Open Access | Times Cited: 153
Bicyclobutanes as unusual building blocks for complexity generation in organic synthesis
Maxim Golfmann, Johannes C. L. Walker
Communications Chemistry (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 137
Maxim Golfmann, Johannes C. L. Walker
Communications Chemistry (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 137
A Practical and Scalable Approach to Fluoro‐Substituted Bicyclo[1.1.1]pentanes
Roman Bychek, Pavel K. Mykhailiuk
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 29
Open Access | Times Cited: 90
Roman Bychek, Pavel K. Mykhailiuk
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 29
Open Access | Times Cited: 90
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: 80
Bethany R. Shire, Edward A. Anderson
JACS Au (2023) Vol. 3, Iss. 6, pp. 1539-1553
Open Access | Times Cited: 80
Synthesis and Applications of Bicyclo[1.1.0]butyl and Azabicyclo[1.1.0]butyl Organometallics
Jasper L. Tyler, Varinder K. Aggarwal
Chemistry - A European Journal (2023) Vol. 29, Iss. 29
Open Access | Times Cited: 45
Jasper L. Tyler, Varinder K. Aggarwal
Chemistry - A European Journal (2023) Vol. 29, Iss. 29
Open Access | Times Cited: 45
Eu(OTf)3‐Catalyzed Formal Dipolar [4π+2σ] Cycloaddition of Bicyclo‐[1.1.0]butanes with Nitrones: Access to Polysubstituted 2‐Oxa‐3‐azabicyclo[3.1.1]heptanes
Jian Zhang, Jia‐Yi Su, Hanliang Zheng, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 13
Closed Access | Times Cited: 45
Jian Zhang, Jia‐Yi Su, Hanliang Zheng, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 13
Closed Access | Times Cited: 45
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: 38
Jet Tsien, Chao Hu, Rohan R. Merchant, et al.
Nature Reviews Chemistry (2024) Vol. 8, Iss. 8, pp. 605-627
Closed Access | Times Cited: 38
Reaction Paradigms that Leverage Cycloaddition and Ring Strain to Construction Bicyclic Aryl Bioisosteres from Bicyclo[1.1.0]butanes
Stephen J. Sujansky, Xiaoshen Ma
Asian Journal of Organic Chemistry (2024) Vol. 13, Iss. 5
Closed Access | Times Cited: 29
Stephen J. Sujansky, Xiaoshen Ma
Asian Journal of Organic Chemistry (2024) Vol. 13, Iss. 5
Closed Access | Times Cited: 29
Strain-release transformations of bicyclo[1.1.0]butanes and [1.1.1]propellanes
Qianqian Hu, Jie Chen, Yang Yang, et al.
Tetrahedron Chem (2024) Vol. 9, pp. 100070-100070
Open Access | Times Cited: 24
Qianqian Hu, Jie Chen, Yang Yang, et al.
Tetrahedron Chem (2024) Vol. 9, pp. 100070-100070
Open Access | Times Cited: 24
Overcoming a Radical Polarity Mismatch in Strain‐Release Pentafluorosulfanylation of [1.1.0]Bicyclobutanes: An Entryway to Sulfone‐ and Carbonyl‐Containing SF5‐Cyclobutanes
Yannick Kraemer, Jón Atiba Buldt, Wang‐Yeuk Kong, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 19
Closed Access | Times Cited: 22
Yannick Kraemer, Jón Atiba Buldt, Wang‐Yeuk Kong, et al.
Angewandte Chemie International Edition (2024) Vol. 63, Iss. 19
Closed Access | Times Cited: 22
Facile Synthesis of Housanes by an Unexpected Strategy
Yanyao Liu, Somanea Tranin, Yu‐Che Chang, et al.
Journal of the American Chemical Society (2025)
Closed Access | Times Cited: 2
Yanyao Liu, Somanea Tranin, Yu‐Che Chang, et al.
Journal of the American Chemical Society (2025)
Closed Access | Times Cited: 2
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: 95
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: 95
Synthesis and Applications of Polysubstituted Bicyclo[1.1.0]butanes
Ryan E. McNamee, Amber L. Thompson, Edward A. Anderson
Journal of the American Chemical Society (2021) Vol. 143, Iss. 50, pp. 21246-21251
Open Access | Times Cited: 65
Ryan E. McNamee, Amber L. Thompson, Edward A. Anderson
Journal of the American Chemical Society (2021) Vol. 143, Iss. 50, pp. 21246-21251
Open Access | Times Cited: 65
Investigating Bicyclobutane–Triazolinedione Cycloadditions as a Tool for Peptide Modification
Brett D. Schwartz, Aidan P. Smyth, Philippe E. Nashar, et al.
Organic Letters (2022) Vol. 24, Iss. 6, pp. 1268-1273
Closed Access | Times Cited: 64
Brett D. Schwartz, Aidan P. Smyth, Philippe E. Nashar, et al.
Organic Letters (2022) Vol. 24, Iss. 6, pp. 1268-1273
Closed Access | Times Cited: 64
Lewis acid-catalyzed diastereoselective carbofunctionalization of bicyclobutanes employing naphthols
Avishek Guin, Subrata Bhattacharjee, Mahesh Singh Harariya, et al.
Chemical Science (2023) Vol. 14, Iss. 24, pp. 6585-6591
Open Access | Times Cited: 41
Avishek Guin, Subrata Bhattacharjee, Mahesh Singh Harariya, et al.
Chemical Science (2023) Vol. 14, Iss. 24, pp. 6585-6591
Open Access | Times Cited: 41
Enantioselective Synthesis of Chiral Cyclobutenes Enabled by Brønsted Acid-Catalyzed Isomerization of BCBs
Si-Li Lin, Ye‐Hui Chen, Huanhuan Liu, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 39, pp. 21152-21158
Closed Access | Times Cited: 40
Si-Li Lin, Ye‐Hui Chen, Huanhuan Liu, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 39, pp. 21152-21158
Closed Access | Times Cited: 40
Stereoselective Alder-Ene Reactions of Bicyclo[1.1.0]butanes: Facile Synthesis of Cyclopropyl- and Aryl-Substituted Cyclobutenes
Ayan Dasgupta, Subrata Bhattacharjee, Zixuan Tong, et al.
Journal of the American Chemical Society (2023) Vol. 146, Iss. 1, pp. 1196-1203
Open Access | Times Cited: 30
Ayan Dasgupta, Subrata Bhattacharjee, Zixuan Tong, et al.
Journal of the American Chemical Society (2023) Vol. 146, Iss. 1, pp. 1196-1203
Open Access | Times Cited: 30
Taming nonclassical carbocations to control small ring reactivity
Ryan E. McNamee, Nils Frank, Kirsten E. Christensen, et al.
Science Advances (2024) Vol. 10, Iss. 2
Open Access | Times Cited: 11
Ryan E. McNamee, Nils Frank, Kirsten E. Christensen, et al.
Science Advances (2024) Vol. 10, Iss. 2
Open Access | Times Cited: 11
Lewis acid-catalyzed diastereoselective formal ene reaction of thioindolinones/thiolactams with bicyclobutanes
Avishek Guin, Shiksha Deswal, Mahesh Singh Harariya, et al.
Chemical Science (2024) Vol. 15, Iss. 31, pp. 12473-12479
Open Access | Times Cited: 11
Avishek Guin, Shiksha Deswal, Mahesh Singh Harariya, et al.
Chemical Science (2024) Vol. 15, Iss. 31, pp. 12473-12479
Open Access | Times Cited: 11
Umpolung reactivity of strained C–C σ-bonds without transition-metal catalysis
Dachang Bai, Xiuli Guo, Xinghua Wang, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9
Dachang Bai, Xiuli Guo, Xinghua Wang, et al.
Nature Communications (2024) Vol. 15, Iss. 1
Open Access | Times Cited: 9
Skeletal Ring Contractions via I(I)/I(III) Catalysis: Stereoselective Synthesis of cis-α,α-Difluorocyclopropanes
Keith Livingstone, Kathrin Siebold, Stephanie Meyer, et al.
ACS Catalysis (2022) Vol. 12, Iss. 23, pp. 14507-14516
Open Access | Times Cited: 31
Keith Livingstone, Kathrin Siebold, Stephanie Meyer, et al.
ACS Catalysis (2022) Vol. 12, Iss. 23, pp. 14507-14516
Open Access | Times Cited: 31
One-Pot Synthesis of Strain-Release Reagents from Methyl Sulfones
Myunggi Jung, Vincent N. G. Lindsay
Journal of the American Chemical Society (2022) Vol. 144, Iss. 11, pp. 4764-4769
Open Access | Times Cited: 28
Myunggi Jung, Vincent N. G. Lindsay
Journal of the American Chemical Society (2022) Vol. 144, Iss. 11, pp. 4764-4769
Open Access | Times Cited: 28
Recent Progress in Accessing Multi-functionalized Caged Hydrocarbons: En Route to Highly Functionalized Saturated (Bio)isosteres of Benzene Rings
Shota Nagasawa, Yoshiharu Iwabuchi
Synthesis (2024)
Closed Access | Times Cited: 7
Shota Nagasawa, Yoshiharu Iwabuchi
Synthesis (2024)
Closed Access | Times Cited: 7
Oxidative sulfonylarylation of strained C–C σ-bonds for the synthesis of 3-spirocyclic oxindoles initiated by insertion of sulfur dioxide
Jian-Hong Fan, Jing Yuan, Long‐Jin Zhong, et al.
Organic Chemistry Frontiers (2024) Vol. 11, Iss. 7, pp. 1982-1989
Closed Access | Times Cited: 6
Jian-Hong Fan, Jing Yuan, Long‐Jin Zhong, et al.
Organic Chemistry Frontiers (2024) Vol. 11, Iss. 7, pp. 1982-1989
Closed Access | Times Cited: 6
Synthesis of Stereodefined Polysubstituted Bicyclo[1.1.0]butanes
Rahul Suresh, Noam Orbach, Ilan Marek
Journal of the American Chemical Society (2024) Vol. 146, Iss. 20, pp. 13748-13753
Open Access | Times Cited: 6
Rahul Suresh, Noam Orbach, Ilan Marek
Journal of the American Chemical Society (2024) Vol. 146, Iss. 20, pp. 13748-13753
Open Access | Times Cited: 6