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- Recent advances in ring-opening of cyclobutanone oximes for capturing SO2, CO or O2
via a radical process. Long-Jin Zhong, Jian-Hong Fan, Pu Chen, Peng-Fei Huang, Bi-Quan Xiong, Ke-Wen Tang, Yu Liu
, Org. Biomol. Chem.
, 2024
, 22
, 10
- Deracemizing organocatalyzed Michael addition reactions of 2-(arylthio)cyclobutanones with β-nitrostyrenes. Alberto Luridiana, Angelo Frongia, David J. Aitken, Regis Guillot, Giorgia Sarais, Francesco Secci
, Org. Biomol. Chem.
, 2016
, 14
, 3394
- Effects of ring-strain on the ultrafast photochemistry of cyclic ketones. Min-Hsien Kao, Ravi Kumar Venkatraman, Michael N. R. Ashfold, Andrew J. Orr-Ewing
, Chem. Sci.
, 2020
, 11
, 1991
- Copper-catalyzed thiocyanation of cyclobutanone oxime esters using ammonium thiocyanate. Xia Zhao, Tengteng Sun, Wenxin Gu, Jingwen Qin, Kui Lu, Fei Ye
, Org. Biomol. Chem.
, 2024
, 22
, 1466
- Visible light-induced palladium-catalyzed ring opening β-H elimination and addition of cyclobutanone oxime esters. Wei-Long Xing, Rui Shang, Guang-Zu Wang, Yao Fu
, Chem. Commun.
, 2019
, 55
, 14291
- Copper-catalyzed tandem aerobic oxidative cyclization for the synthesis of 4-cyanoalkylpyrrolo[1,2-a]quinoxalines from 1-(2-aminophenyl)pyrroles and cyclobutanone oxime esters. Zhenyu An, Yong Jiang, Xin Guan, Rulong Yan
, Chem. Commun.
, 2018
, 54
, 10738
- Synthesis and applications of rhodacyclopentanones derived from C–C bond activation. Megan H. Shaw, John F. Bower
, Chem. Commun.
, 2016
, 52
, 10817
- Ni-Catalyzed radical cyclization of vinyl azides with cyclobutanone oxime esters to access cyanoalkyl containing quinoxalin-2(1H)-ones. Nengneng Zhou, Sixin Wu, Kaimo Kuang, Meixia Wu, Man Zhang
, Org. Biomol. Chem.
, 2021
, 19
, 4697
- Structure of the B state of cyclobutanone. Fabio Momicchioli, Ivan Baraldi, Gianfranco Di Lonardo
, J. Chem. Soc., Faraday Trans. 2
, 1975
, 71
, 791
- Organophotocatalytic cascade cyclization reactions for the synthesis of cyanoalkyl indole[2,1-a]isoquinolinones. Dong-Liang Zhang, Zhi-Qiang Zhu, Zong-Bo Xie, Xiao-Ping Zhang, Zhang-Gao Le
, New J. Chem.
, 2023
, 47
, 18354