Reactions of nitroxides 15. Cinnamates bearing a nitroxyl moiety synthesized using a Mizoroki–Heck cross-coupling reaction

Jerzy Zakrzewski and Bogumiła Huras
Beilstein J. Org. Chem. 2015, 11, 1155–1162. https://doi.org/10.3762/bjoc.11.130

Supporting Information

Supporting Information File 1: EIMS, ESIMS, 1H NMR, 13C NMR, and IR spectra of 3 and 5a5i.
Format: PDF Size: 3.1 MB Download

Cite the Following Article

Reactions of nitroxides 15. Cinnamates bearing a nitroxyl moiety synthesized using a Mizoroki–Heck cross-coupling reaction
Jerzy Zakrzewski and Bogumiła Huras
Beilstein J. Org. Chem. 2015, 11, 1155–1162. https://doi.org/10.3762/bjoc.11.130

How to Cite

Zakrzewski, J.; Huras, B. Beilstein J. Org. Chem. 2015, 11, 1155–1162. doi:10.3762/bjoc.11.130

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

  • Kustin, R. P.; Levin, O. V.; Filippova, S. S.; Alekseeva, E. V. Bis(2,2,6,6-tetramethyl-1-(λ1-oxidaneyl)piperidin-4-yl) 3,3′-((2-hydroxyethyl)azanediyl)dipropionate. Molbank 2024, 2024, M1788. doi:10.3390/m1788
  • Prekob, Á.; Szamosvölgyi, Á.; Muránszky, G.; Lakatos, J.; Kónya, Z.; Fiser, B.; Viskolcz, B.; Vanyorek, L. Palladium Decorated N-Doped Carbon Foam as a Highly Active and Selective Catalyst for Nitrobenzene Hydrogenation. International journal of molecular sciences 2022, 23, 6423. doi:10.3390/ijms23126423
  • Gu, C.; Zhang, Q.; Li, Y.; Li, R.; Feng, J.; Chen, W.; Ahmed, W.; Soufiany, I.; Huang, S.; Long, J.; Chen, L. The PI3K/AKT Pathway-The Potential Key Mechanisms of Traditional Chinese Medicine for Stroke. Frontiers in medicine 2022, 9, 900809. doi:10.3389/fmed.2022.900809
  • Bobbitt, J. M.; Eddy, N. A.; Cady, C. X.; Jin, J.; Gascón, J. A.; Gelpí-Domínguez, S.; Zakrzewski, J.; Morton, M. D. Preparation of Some Homologous TEMPO Nitroxides and Oxoammonium Salts; Notes on the NMR Spectroscopy of Nitroxide Free Radicals; Observed Radical Nature of Oxoammonium Salt Solutions Containing Trace Amounts of Corresponding Nitroxides in an Equilibrium Relationship. The Journal of organic chemistry 2017, 82, 9279–9290. doi:10.1021/acs.joc.7b00846
  • Poater, A.; Vummaleti, S. V. C.; Polo, A.; Cavallo, L. Clean and selective catalytic C-H alkylation of alkenes with environmental friendly alcohols. Molecular Catalysis 2017, 435, 69–75. doi:10.1016/j.molcata.2016.09.010
  • Bognár, B.; Varga, B.; Kálai, T.; Csokona, V.; Fekete, G. G.; Sár, C. P.; Hideg, K. Reaction of β-Bromo-β,γ-unsaturated Pyrroline Nitroxide Aldehydes and Nitriles with Aromatic N,S-Binucleophiles. Journal of Heterocyclic Chemistry 2017, 54, 2556–2562. doi:10.1002/jhet.2850
  • Chen, H.; Tan, G.; Cao, J.; Zhang, G.; Peng, Y.; Yu, P.; Sun, Y.; Zhang, Z.; Wang, Y. Design, Synthesis, and Biological Evaluation of Novel Tetramethylpyrazine Derivatives as Potential Neuroprotective Agents. Chemical & pharmaceutical bulletin 2016, 65, 56–65. doi:10.1248/cpb.c16-00699
  • Poater, A.; Vummaleti, S. V. C.; Polo, A.; Cavallo, L. Mechanistic Insights of a Selective C-H Alkylation of Alkenes by a Ru–based Catalyst and Alcohols. ChemistrySelect 2016, 1, 4218–4228. doi:10.1002/slct.201600860
  • Zakrzewski, J.; Huras, B. Reactions of Nitroxides. Part 15. Cinnamates Bearing a Nitroxyl Moiety Synthesized Using a Mizoroki—Heck Cross‐Coupling Reaction. ChemInform 2015, 46. doi:10.1002/chin.201537171
Other Beilstein-Institut Open Science Activities