References
- Fey, T.; Fischer, H.; Bachmann, S.; Albert, K.; Bolm, C. J. Org. Chem. 2001, 99, 8154.
- Dlugosz, D.; Pach, M.; Zabrzenska, A.; Zegar, M.; Oleksyn, B. J.; Kalinowska-Tluscik, J.; Ostrowska, K. Monatsh Chem. 2008, 139, 543. https://doi.org/10.1007/s00706-007-0788-x
- Fieser, L. F.; Fieser, M. Reagents for Organic Synthesis; Wiley and Sons Inc.: New York, 1967; p 967.
- Kavala, V.; Naik, S.; Patel. B. K. J. Org. Chem. 2005, 70, 4267. https://doi.org/10.1021/jo050059u
- Bekaert, A.; Provot, O.; Rasolojaona, O.; Alami, M.; Brion, J. D. Tetrahedron Lett. 2005, 46, 4187. https://doi.org/10.1016/j.tetlet.2005.04.049
- Zhang, S. J.; Le, Z. Chin. Chem. Lett. 2005, 16, 1590.
- Giordano, C.; Coppi, L. J. Org. Chem. 1992, 57, 2765. https://doi.org/10.1021/jo00036a001
- Bellucci, G.; Bianchini, R.; Ambrosetti, R. J. Chem. Soc. Perkin Trans. 2 1987, 39.
- Bellucci, G.; Chiappe, C.; Dandrea, F. Tetrahedron: Asymmetry 1995, 6, 221. https://doi.org/10.1016/0957-4166(94)00378-O
- Bellucci, G.; Bianchini, R.; Ambrosetti, R.; Ingrosso, G. J. Org. Chem. 1985, 50, 3313. https://doi.org/10.1021/jo00218a013
- Bellucci, G.; Bianchini, R.; Chiappe, C. J. Org. Chem. 1991, 56,3067. https://doi.org/10.1021/jo00009a027
- Chaudhuri, M. K.; Khan, A. T.; Patel, B. K. Tetrahedron Lett. 1998,39, 8163. https://doi.org/10.1016/S0040-4039(98)01818-8
- Bose, G.; Mondal, E.; Khan, A. T.; Bordoloi, M. J. Tetrahedron Lett. 2001, 42, 8907. https://doi.org/10.1016/S0040-4039(01)01938-4
- Mohr, P. J.; Halcomb, R. L. Org. Lett. 2002, 4, 2413. https://doi.org/10.1021/ol026159t
- Muathen, H. A. J. Org. Chem. 1992, 57, 2740. https://doi.org/10.1021/jo00035a038
- Le, Z. G.; Chen, Z. C.; Hu, Y.; Zheng, Q. G. Chin. Chem. Lett. 2005,16, 1007.
- Cerichelli, G.; Lucheti, L.; Mancini, G. Tetrahedron 1996, 52,2465. https://doi.org/10.1016/0040-4020(95)01067-X
- Bora, U.; Bose, G.; Chaudhuri, M. K.; Dhar, S. S.; Gopinath, R.;Khan, A. T.; Patel, B. K. Org. Lett. 2000, 2, 247. https://doi.org/10.1021/ol9902935
- Singhal, S.; Jain, S. L.; Sain, B. J. Mol. Catal. A: Chem. 2006, 258,198. https://doi.org/10.1016/j.molcata.2006.05.042
- Joseph, J. K.; Jain, S. L.; Sain, B. Catal. Commun. 2007, 8, 83. https://doi.org/10.1016/j.catcom.2006.05.035
- Aoyama, T.; Takido, T.; Kodomari, M. Tetrahedron Lett. 2005, 46,1989. https://doi.org/10.1016/j.tetlet.2005.01.159
- Kar, G.; Saikia, A. K.; Bora, U.; Dehury, S. K.; Chaudhuri, M. K.Tetrahedron Lett. 2003, 44, 4503. https://doi.org/10.1016/S0040-4039(03)01015-3
- Mondal, E.; Sahu, P. R.; Bose, G.; Khan, A. T. Tetrahedron Lett.2002, 43, 2843. https://doi.org/10.1016/S0040-4039(02)00345-3
- Naik, S.; Gopinath, R.; Patel, B. K. Tetrahedron Lett. 2001, 42,7679. https://doi.org/10.1016/S0040-4039(01)01599-4
- Gopinath, R.; Patel, B. K. Org. Lett. 2000, 2, 4177. https://doi.org/10.1021/ol006720s
- Lakouraj, M. M.; Ghodrati, K. Monatsh Chem. 2008, 139, 549. https://doi.org/10.1007/s00706-007-0787-y
- Ali, S. I.; Nikalje, M. D.; Sudalai, A. Org. Lett. 1999, 1, 705. https://doi.org/10.1021/ol9900966
- Jordan, A. D.; Luo, C.; Reitz, A. B. J. Org. Chem. 2003, 68, 8693. https://doi.org/10.1021/jo0349431
- Sharghi, H.; Massah. A. R.; Eshghi, H.; Niknam, K. J. Org. Chem.1998, 63, 1455. https://doi.org/10.1021/jo971453y
- Sharghi, H.; Niknam, K.; Pooyan, M. Tetrahedron 2001, 57, 6057. https://doi.org/10.1016/S0040-4020(01)00443-4
- Sharghi, H.; Niknam, K, Bull. Chem. Soc. Jpn. 1999, 72, 1525. https://doi.org/10.1246/bcsj.72.1525
- Sharghi, H.; Niknam, K. J. Chem. Res. (S) 1999, 310.
- Aggarwal, V. K.; Mereu, A. J. Org. Chem. 2000, 65, 7211. https://doi.org/10.1021/jo000584n
- The data can be obtained free of charge via http://www.ccdc.cam.ac.uk/perl/catreq.cgi (or from the CCDC, 12 Union Road, Cambridge CB2 1EZ, UK; fax: +44 1223 336033; e-mail: deposit @ccdc.cam.ac.uk).
Cited by
- DBU-Promoted Nucleophilic Activation of Carbonic Acid Diesters vol.2011, pp.13, 2011, https://doi.org/10.1002/ejoc.201001725
- A Simple and Efficient Chemical Decontamination of Sulfur Mustard (HD) Using 1,8-Diazabicyclo[5,4,0]Undec-7-Ene Hydrobromide-Perbromide vol.187, pp.2, 2012, https://doi.org/10.1080/10426507.2011.600742
- as a New and Efficient Oxidant vol.33, pp.2, 2012, https://doi.org/10.5012/bkcs.2012.33.2.515
- 1,8-Diazabicyclo[5.4.0] Undec-7-Ene -Hydrobromide-Perbromide: An Oxidising Agent for One-Pot Oxidative Esterification of Aldehydes vol.35, pp.10, 2010, https://doi.org/10.3184/174751911x13178067432066
- P2O5/SiO2 as an Efficient and Mild Catalyst for Trimethylsilylation of Alcohols Using Hexamethyldisilazane vol.42, pp.10, 2010, https://doi.org/10.1080/15533174.2012.682686
- Fe(HSO4)3 as an Efficient Catalyst for Diazotization and Diazo Coupling Reactions vol.56, pp.6, 2010, https://doi.org/10.5012/jkcs.2012.56.6.716
- Dabco Ammonium Halochromates, $$ {\text{C}}_{6} {\text{H}}_{14} {\text{N}}_{2}\,^{ + } $$ C 6 H 14 N 2 + $$ {\text{Cr}}_{2} {\text{F}}_{2} {\text{O}}_{6}\,^{ - } $$ Cr 2 F 2 O 6 - (DAXC, X = F, Cl), R vol.42, pp.3, 2010, https://doi.org/10.1007/s40995-018-0497-9