
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:
Intermolecular [2π+2σ]-photocycloaddition enabled by triplet energy transfer
Roman Kleinmans, Tobias Pinkert, Subhabrata Dutta, et al.
Nature (2022) Vol. 605, Iss. 7910, pp. 477-482
Closed Access | Times Cited: 239
Roman Kleinmans, Tobias Pinkert, Subhabrata Dutta, et al.
Nature (2022) Vol. 605, Iss. 7910, pp. 477-482
Closed Access | Times Cited: 239
Showing 1-25 of 239 citing articles:
Strain-Release [2π + 2σ] Cycloadditions for the Synthesis of Bicyclo[2.1.1]hexanes Initiated by Energy Transfer
Renyu Guo, Yu‐Che Chang, Loïc Herter, et al.
Journal of the American Chemical Society (2022) Vol. 144, Iss. 18, pp. 7988-7994
Open Access | Times Cited: 179
Renyu Guo, Yu‐Che Chang, Loïc Herter, et al.
Journal of the American Chemical Society (2022) Vol. 144, Iss. 18, pp. 7988-7994
Open Access | Times Cited: 179
A catalytic alkene insertion approach to bicyclo[2.1.1]hexane bioisosteres
Soumitra Agasti, Frédéric Beltran, Emma Pye, et al.
Nature Chemistry (2023) Vol. 15, Iss. 4, pp. 535-541
Closed Access | Times Cited: 155
Soumitra Agasti, Frédéric Beltran, Emma Pye, et al.
Nature Chemistry (2023) Vol. 15, Iss. 4, pp. 535-541
Closed Access | Times Cited: 155
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: 143
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: 143
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
Nils Frank, Jeremy Nugent, Bethany R. Shire, et al.
Nature (2022) Vol. 611, Iss. 7937, pp. 721-726
Closed Access | Times Cited: 135
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: 132
Maxim Golfmann, Johannes C. L. Walker
Communications Chemistry (2023) Vol. 6, Iss. 1
Open Access | Times Cited: 132
Photochemical Intermolecular [3σ + 2σ]-Cycloaddition for the Construction of Aminobicyclo[3.1.1]heptanes
Yongxiang Zheng, Weichen Huang, Roshan K. Dhungana, et al.
Journal of the American Chemical Society (2022) Vol. 144, Iss. 51, pp. 23685-23690
Open Access | Times Cited: 130
Yongxiang Zheng, Weichen Huang, Roshan K. Dhungana, et al.
Journal of the American Chemical Society (2022) Vol. 144, Iss. 51, pp. 23685-23690
Open Access | Times Cited: 130
Beyond Bioisosteres: Divergent Synthesis of Azabicyclohexanes and Cyclobutenyl Amines from Bicyclobutanes**
Kushal Dhake, Kyla Woelk, Joseph Becica, et al.
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 27
Closed Access | Times Cited: 126
Kushal Dhake, Kyla Woelk, Joseph Becica, et al.
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 27
Closed Access | Times Cited: 126
Energy-Transfer-Enabled Dearomative Cycloaddition Reactions of Indoles/Pyrroles via Excited-State Aromatics
Min Zhu, Xiǎo Zhang, Chao Zheng, et al.
Accounts of Chemical Research (2022) Vol. 55, Iss. 17, pp. 2510-2525
Closed Access | Times Cited: 121
Min Zhu, Xiǎo Zhang, Chao Zheng, et al.
Accounts of Chemical Research (2022) Vol. 55, Iss. 17, pp. 2510-2525
Closed Access | Times Cited: 121
Synthesis of Polysubstituted 2-Oxabicyclo[2.1.1]hexanes via Visible-Light-Induced Energy Transfer
Yujie Liang, Roman Kleinmans, Constantin G. Daniliuc, et al.
Journal of the American Chemical Society (2022) Vol. 144, Iss. 44, pp. 20207-20213
Closed Access | Times Cited: 119
Yujie Liang, Roman Kleinmans, Constantin G. Daniliuc, et al.
Journal of the American Chemical Society (2022) Vol. 144, Iss. 44, pp. 20207-20213
Closed Access | Times Cited: 119
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: 118
Peter Bellotti, Frank Glorius
Journal of the American Chemical Society (2023) Vol. 145, Iss. 38, pp. 20716-20732
Closed Access | Times Cited: 118
Enantioselective [2+2]-cycloadditions with triplet photoenzymes
Ningning Sun, Jianjian Huang, Junyi Qian, et al.
Nature (2022) Vol. 611, Iss. 7937, pp. 715-720
Closed Access | Times Cited: 117
Ningning Sun, Jianjian Huang, Junyi Qian, et al.
Nature (2022) Vol. 611, Iss. 7937, pp. 715-720
Closed Access | Times Cited: 117
Selective [2σ + 2σ] Cycloaddition Enabled by Boronyl Radical Catalysis: Synthesis of Highly Substituted Bicyclo[3.1.1]heptanes
Tao Yu, Jinbo Yang, Zhijun Wang, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 7, pp. 4304-4310
Closed Access | Times Cited: 116
Tao Yu, Jinbo Yang, Zhijun Wang, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 7, pp. 4304-4310
Closed Access | Times Cited: 116
A designed photoenzyme for enantioselective [2+2] cycloadditions
Jonathan S. Trimble, Rebecca Crawshaw, Florence J. Hardy, et al.
Nature (2022) Vol. 611, Iss. 7937, pp. 709-714
Open Access | Times Cited: 114
Jonathan S. Trimble, Rebecca Crawshaw, Florence J. Hardy, et al.
Nature (2022) Vol. 611, Iss. 7937, pp. 709-714
Open Access | Times Cited: 114
Energy transfer photocatalysis: exciting modes of reactivity
Subhabrata Dutta, Johannes E. Erchinger, Felix Strieth‐Kalthoff, et al.
Chemical Society Reviews (2024) Vol. 53, Iss. 3, pp. 1068-1089
Closed Access | Times Cited: 113
Subhabrata Dutta, Johannes E. Erchinger, Felix Strieth‐Kalthoff, et al.
Chemical Society Reviews (2024) Vol. 53, Iss. 3, pp. 1068-1089
Closed Access | Times Cited: 113
ortho-Selective Dearomative [2π + 2σ] Photocycloadditions of Bicyclic Aza-Arenes
Roman Kleinmans, Subhabrata Dutta, Kristers Ozols, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 22, pp. 12324-12332
Closed Access | Times Cited: 111
Roman Kleinmans, Subhabrata Dutta, Kristers Ozols, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 22, pp. 12324-12332
Closed Access | Times Cited: 111
Lewis Acid Catalyzed Formal (3+2)‐Cycloaddition of Bicyclo[1.1.0]butanes with Ketenes
Niklas Radhoff, Constantin G. Daniliuc, Armido Studer
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 34
Open Access | Times Cited: 107
Niklas Radhoff, Constantin G. Daniliuc, Armido Studer
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 34
Open Access | Times Cited: 107
Diboron(4)‐Catalyzed Remote [3+2] Cycloaddition of Cyclopropanes via Dearomative/Rearomative Radical Transmission through Pyridine
Ming Xu, Zhijun Wang, Zhaohui Sun, et al.
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 52
Closed Access | Times Cited: 102
Ming Xu, Zhijun Wang, Zhaohui Sun, et al.
Angewandte Chemie International Edition (2022) Vol. 61, Iss. 52
Closed Access | Times Cited: 102
Dearomative ring expansion of thiophenes by bicyclobutane insertion
Huamin Wang, Huiling Shao, Ankita Das, et al.
Science (2023) Vol. 381, Iss. 6653, pp. 75-81
Closed Access | Times Cited: 102
Huamin Wang, Huiling Shao, Ankita Das, et al.
Science (2023) Vol. 381, Iss. 6653, pp. 75-81
Closed Access | Times Cited: 102
Pyridine-Boryl Radical-Catalyzed [2π + 2σ] Cycloaddition of Bicyclo[1.1.0]butanes with Alkenes
Yuan Liu, Shuang Lin, Yin Li, et al.
ACS Catalysis (2023) Vol. 13, Iss. 7, pp. 5096-5103
Open Access | Times Cited: 101
Yuan Liu, Shuang Lin, Yin Li, et al.
ACS Catalysis (2023) Vol. 13, Iss. 7, pp. 5096-5103
Open Access | Times Cited: 101
Catalytic Formal [2π+2σ] Cycloaddition of Aldehydes with Bicyclobutanes: Expedient Access to Polysubstituted 2‐Oxabicyclo[2.1.1]hexanes
Yujie Liang, Fritz Paulus, Constantin G. Daniliuc, et al.
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 34
Closed Access | Times Cited: 99
Yujie Liang, Fritz Paulus, Constantin G. Daniliuc, et al.
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 34
Closed Access | Times Cited: 99
General access to cubanes as benzene bioisosteres
Mario P. Wiesenfeldt, James A. Rossi‐Ashton, Ian B. Perry, et al.
Nature (2023) Vol. 618, Iss. 7965, pp. 513-518
Open Access | Times Cited: 92
Mario P. Wiesenfeldt, James A. Rossi‐Ashton, Ian B. Perry, et al.
Nature (2023) Vol. 618, Iss. 7965, pp. 513-518
Open Access | Times Cited: 92
2-Oxabicyclo[2.1.1]hexanes as saturated bioisosteres of the ortho-substituted phenyl ring
Aleksandr Denisenko, Pavel Garbuz, Nataliya M. Voloshchuk, et al.
Nature Chemistry (2023) Vol. 15, Iss. 8, pp. 1155-1163
Open Access | Times Cited: 88
Aleksandr Denisenko, Pavel Garbuz, Nataliya M. Voloshchuk, et al.
Nature Chemistry (2023) Vol. 15, Iss. 8, pp. 1155-1163
Open Access | Times Cited: 88
Photocatalyzed [2σ + 2σ] and [2σ + 2π] Cycloadditions for the Synthesis of Bicyclo[3.1.1]heptanes and 5- or 6-Membered Carbocycles
Tin V. T. Nguyen, André Bossonnet, Matthew D. Wodrich, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 46, pp. 25411-25421
Open Access | Times Cited: 84
Tin V. T. Nguyen, André Bossonnet, Matthew D. Wodrich, et al.
Journal of the American Chemical Society (2023) Vol. 145, Iss. 46, pp. 25411-25421
Open Access | Times Cited: 84
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
Bethany R. Shire, Edward A. Anderson
JACS Au (2023) Vol. 3, Iss. 6, pp. 1539-1553
Open Access | Times Cited: 73
Intermolecular Formal Cycloaddition of Indoles with Bicyclo[1.1.0]butanes by Lewis Acid Catalysis
Dongshun Ni, Sai Hu, Xiangyu Tan, et al.
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 48
Open Access | Times Cited: 72
Dongshun Ni, Sai Hu, Xiangyu Tan, et al.
Angewandte Chemie International Edition (2023) Vol. 62, Iss. 48
Open Access | Times Cited: 72