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- Rationalizing the diverse reactivity of [1.1.1]propellane through σ–π-delocalization. Alistair J. Sterling, Alexander B. Dürr, Russell C. Smith, Edward A. Anderson, Fernanda Duarte
, Chem. Sci.
, 2020
, 11
, 4895
- Synthesis and applications of highly functionalized 1-halo-3-substituted bicyclo[1.1.1]pentanes. Dimitri F. J. Caputo, Carlos Arroniz, Alexander B. Dürr, James J. Mousseau, Antonia F. Stepan, Steven J. Mansfield, Edward A. Anderson
, Chem. Sci.
, 2018
, 9
, 5295
- Strain release – an old tool for new transformations. Joanna Turkowska, Jakub Durka, Dorota Gryko
, Chem. Commun.
, 2020
, 56
, 5718
- Halogen bond shortens and strengthens the bridge bond of [1.1.1]propellane and the open form of [2.2.2]propellane. Jyothish Joy, Edakkandy Akhil, Eluvathingal D. Jemmis
, Phys. Chem. Chem. Phys.
, 2018
, 20
, 25792
- Ab initio calculations of the NMR spectra of [1.1.1]propellane and bicyclo[1.1.1]pentane. Magdalena Pecul, Helena Dodziuk, Michał Jaszuński, Oleg Lukin, Jerzy Leszczyński
, Phys. Chem. Chem. Phys.
, 2001
, 3
, 1986
- Visible-light-induced direct perfluoroalkylation/heteroarylation of [1.1.1]propellane to diverse bicyclo[1.1.1]pentanes (BCPs) under metal and photocatalyst-free conditions. Jiashun Zhu, Yirui Guo, Yuru Zhang, Wanmei Li, Pengfei Zhang, Jun Xu
, Green Chem.
, 2023
, 25
, 986
- Photoinduced strategies towards strained molecules. Mukund M. D. Pramanik, Hao Qian, Wen-Jing Xiao, Jia-Rong Chen
, Org. Chem. Front.
, 2020
, 7
, 2531
- A continuous flow synthesis of [1.1.1]propellane and bicyclo[1.1.1]pentane derivatives. Kian Donnelly, Marcus Baumann
, Chem. Commun.
, 2021
, 57
, 2871
- High-resolution electron momentum spectroscopy of molecules. Michael J. Brunger, William Adcock
, J. Chem. Soc., Perkin Trans. 2
, 2002
, 1
- Synthesis of C3-halo substituted bicyclo[1.1.1]pentylamines via halosulfoamidation of [1.1.1]propellane with sodium hypohalites and sulfonamides. Zhi Li, Deyou Lan, Wei Zhou, Jiacheng Li, Hui Zhu, Chuanming Yu, Xinpeng Jiang
, Chem. Commun.
, 2023
, 59
, 6056