Supporting Information
| Supporting Information File 1: Additional data. | ||
| Format: PDF | Size: 623.3 KB | Download |
Cite the Following Article
Ring opening of 2-aza-3-borabicyclo[2.2.0]hex-5-ene, the Dewar form of 1,2-dihydro-1,2-azaborine: stepwise versus concerted mechanisms
Holger F. Bettinger and Otto Hauler
Beilstein J. Org. Chem. 2013, 9, 761–766.
https://doi.org/10.3762/bjoc.9.86
How to Cite
Bettinger, H. F.; Hauler, O. Beilstein J. Org. Chem. 2013, 9, 761–766. doi:10.3762/bjoc.9.86
Download Citation
Citation data can be downloaded as file using the "Download" button or used for copy/paste from the text window
below.
Citation data in RIS format can be imported by all major citation management software, including EndNote,
ProCite, RefWorks, and Zotero.
Citations to This Article
Up to 20 of the most recent references are displayed here.
Scholarly Works
- Han, G.; Wei, H.; Yu, X.; Zhang, J.; Ma, Y.; Liu, P. A different view on the deactivation process of 3-hydroxy-salicylidene-methylamine system. Chemical Physics Letters 2024, 835, 141004. doi:10.1016/j.cplett.2023.141004
- Jeong, S.; Park, E.; Kim, J.; Kim, K. H. Ultrafast photoisomerization mechanism of azaborine revealed by nonadiabatic molecular dynamics simulations. Physical chemistry chemical physics : PCCP 2023, 25, 17230–17237. doi:10.1039/d3cp01169k
- Zhao, L.; Liu, J.; Zhou, P. The photoinduced isomerization mechanism of the 2-(1-(methylimino)methyl)-6-chlorophenol (SMAC): Nonadiabatic surface hopping dynamics simulations. The Journal of chemical physics 2018, 149, 034309. doi:10.1063/1.5034379
- Edel, K.; Yang, X.; Ishibashi, J. S. A.; Lamm, A. N.; Maichle‐Mössmer, C.; Giustra, Z. X.; Liu, S.; Bettinger, H. F. The Dewar Isomer of 1,2‐Dihydro‐1,2‐azaborinines: Isolation, Fragmentation, and Energy Storage. Angewandte Chemie 2018, 130, 5394–5398. doi:10.1002/ange.201712683
- Edel, K.; Yang, X.; Ishibashi, J. S. A.; Lamm, A. N.; Maichle-Mössmer, C.; Giustra, Z. X.; Liu, S.-Y.; Bettinger, H. F. The Dewar Isomer of 1,2‐Dihydro‐1,2‐azaborinines: Isolation, Fragmentation, and Energy Storage. Angewandte Chemie (International ed. in English) 2018, 57, 5296–5300. doi:10.1002/anie.201712683
- Bélanger-Chabot, G.; Braunschweig, H.; Roy, D. K. Recent Developments in Azaborinine Chemistry. European Journal of Inorganic Chemistry 2017, 2017, 4353–4368. doi:10.1002/ejic.201700562
- Edel, K.; Brough, S. A.; Lamm, A. N.; Liu, S.-Y.; Bettinger, H. F. 1,2-Azaborine: The Boron-Nitrogen Derivative of ortho-Benzyne. Angewandte Chemie (International ed. in English) 2015, 54, 7819–7822. doi:10.1002/anie.201502967
- Edel, K.; Brough, S. A.; Lamm, A. N.; Liu, S.; Bettinger, H. F. 1,2‐Azaborine: The Boron‐Nitrogen Derivative of ortho‐Benzyne. Angewandte Chemie 2015, 127, 7930–7933. doi:10.1002/ange.201502967
- Kim, J.; Moon, J.; Lim, J. S. Theoretical Investigation of the Reaction Mechanism of the Photoisomerization of 1,2-Dihydro-1,2-azaborine. Chemphyschem : a European journal of chemical physics and physical chemistry 2015, 16, 1670–1675. doi:10.1002/cphc.201500153
