Bulletin of the Korean Chemical Society

Korean Chemical Society (대한화학회)
권호 표지
DOI QR코드

DOI QR Code

New Synthesis and Nitration of 1,2-Bis(5-aminotetrazol-1-yl)ethane

  • Received : 2011.10.31
  • Accepted : 2011.12.07
  • Published : 2012.02.20
Download PDF
⟨ Previous Next ⟩

Abstract

Keywords

References

  1. Gao, H.; Shreeve, J. M. Chem. Rev. 2011, 111, 7377. https://doi.org/10.1021/cr200039c
  2. Klapotke, T. M.; Sabate, C. M.; Rusan, M. Z. Anorg. Allg. Chem. 2008, 634, 1867. https://doi.org/10.1002/zaac.200800228
  3. Jin, C.-M.; Ye, C.; Piekarski, C.; Twamley, B.; Shreeve, J. M. Eur. J. Inorg. Chem. 2005, 3760.
  4. Gao, Y.; Ye, C.; Twamley, B.; Shreeve, J. M. Chem. Eur. J. 2006, 12, 9010. https://doi.org/10.1002/chem.200600354
  5. Klapotke, T. M.; Sabate, C. M. Chem. Mater. 2008, 20, 1750. https://doi.org/10.1021/cm703344h
  6. Klapotke, T. M.; Sabate, C. M. Chem. Mater. 2008, 20, 3629. https://doi.org/10.1021/cm703657k
  7. Klapotke, T. M.; Sabate, C. M.; Welch, J. M. Z. Anorg. Allg. Chem. 2008, 634, 857. https://doi.org/10.1002/zaac.200700539
  8. Klapotke, T. M.; Sabate, C. M.; Stierstorfer, J. New J. Chem. 2009, 33, 136. https://doi.org/10.1039/b812529e
  9. Klapotke, T. M.; Sabate, C. M. Dalton Trans. 2009, 1835.
  10. Joo, Y.-H.; Shreeve, J. M. Angew. Chem. Int. Ed. 2009, 48, 564. https://doi.org/10.1002/anie.200804755
  11. Joo, Y.-H.; Shreeve, J. M. Chem. Eur. J. 2009, 15, 3198. https://doi.org/10.1002/chem.200802326
  12. Joo, Y.-H.; Shreeve, J. M. J. Am. Chem. Soc. 2010, 132, 15081. https://doi.org/10.1021/ja107729c
  13. Barmin, M. I.; Gromova, S. A.; Mel'nikov, V. V. Russ. J. Appl. Chem. 2001, 74, 1156. https://doi.org/10.1023/A:1013075119625
  14. Joo, Y.-H.; Shreeve, J. M. Org. Lett. 2008, 10, 4665. https://doi.org/10.1021/ol8019742
  15. Joo, Y.-H.; Shreeve, J. M. Eur. J. Org. Chem. 2009, 3573-3578.
  16. Joo, Y.-H.; Shreeve, J. M. Angew. Chem. Int. Ed. 2010, 49, 7320-7323. https://doi.org/10.1002/anie.201003866
  17. Marsh, F. D.; Hermes, M. E. J. Am. Chem. Soc. 1964, 86, 4506. https://doi.org/10.1021/ja01074a071
  18. Marsh, F. D. J. Org. Chem. 1972, 37, 2966. https://doi.org/10.1021/jo00984a012
  19. Joo, Y.- H.; Twamley, B.; Garg, S.; Shreeve, J. M. Angew. Chem. Int. Ed. 2008, 47, 6236. https://doi.org/10.1002/anie.200801886
  20. Stolle, R.; Ehrmann, K.; Rieder, D.; Wille, H.; Winter, H.; Henke- Stark, F. J. Prakt. Chem. 1932, 134, 282. https://doi.org/10.1002/prac.19321340902
  21. Finnegan, W. G.; Henry, R. A. J. Org. Chem. 1959, 24, 1565. https://doi.org/10.1021/jo01092a602

Cited by

  1. Synthesis and Characterization of Bisimidazolylfuroxan Derivatives vol.34, pp.6, 2013, https://doi.org/10.5012/bkcs.2013.34.6.1864
  2. ′-Ethylene-Bridged Bis(nitropyrazoles): Diversified Functionalities and Properties vol.20, pp.50, 2014, https://doi.org/10.1002/chem.201404991
  3. Synthesis and Characterization of BNFF Analogues vol.33, pp.8, 2012, https://doi.org/10.5012/bkcs.2012.33.8.2765
  4. Synthesis of nitrogen-rich imidazole, 1,2,4-triazole and tetrazole-based compounds vol.4, pp.14, 2014, https://doi.org/10.1039/c3ra47227b
  5. Bis(nitroamino‐1,2,4‐triazolates): N‐Bridging Strategy Toward Insensitive Energetic Materials vol.126, pp.47, 2012, https://doi.org/10.1002/ange.201408127
  6. Bis(nitroamino‐1,2,4‐triazolates): N‐Bridging Strategy Toward Insensitive Energetic Materials vol.53, pp.47, 2012, https://doi.org/10.1002/anie.201408127