References
- Uemura, S.; Hirai, Y.; Ohe, K.; Sugiti, N. J. Chem. Soc., Chem. Commun. 1985, 1037-1038.
- Lenardão, E. J.; Mendes, S. R.; Ferreira, P. C.; Perin, G.; Silveira, C. C.; Jacob, R. G. Tetrahedron Lett. 2006, 47, 7439-7442. https://doi.org/10.1016/j.tetlet.2006.08.049
- Nicolaou, K. C.; Petasis, N. A. In Selenium in Natural Products Synthesis; CIS: Pennsylvania, 1984.
- Krief, A.; Derock, M. Tetrahedron Lett. 2002, 43, 3083. https://doi.org/10.1016/S0040-4039(02)00277-0
- Ranu, B. C.; Mandal, T. Tetrahedron Lett. 2006, 47, 5677-5680. https://doi.org/10.1016/j.tetlet.2006.06.012
- Braga, A. L.; Schneider, P. H.; Paixão, M. W.; Deobald, A. M. Tetrahedron Lett. 2006, 47, 7195-7198. https://doi.org/10.1016/j.tetlet.2006.07.148
- Zhao, X.; Yu, Z.; Yan, S.; Wu, S.; Liu, R.; He, W.; Wang, L. J. Org. Chem. 2005, 70, 7338-7341. https://doi.org/10.1021/jo051015o
- Movassagh, B.; Shamsipoor, M. Synlett 2005, 121-122.
- Cohen, R. J.; Fox, D. L. J. Org. Chem. 2004, 69, 4265-4268. https://doi.org/10.1021/jo0401265
- Munbunjong, W.; Lee, E. H.; Chavasiri, W.; Jang, D. O. Tetrahedron Lett. 2005, 46, 8769-8771. https://doi.org/10.1016/j.tetlet.2005.10.025
- Munbunjong, W.; Lee. E. H.; Ngernmaneerat, P.; Kim, S. J.; Singh, G.; Chavasiri, W.; Jang, D. O. Tetrahedron 2009, 65, 2467-2471. https://doi.org/10.1016/j.tet.2009.01.072
- Ikegai, K.; Pluempanupat, W.; Mukaiyama, T. Chem. Lett. 2005, 34, 638-639. https://doi.org/10.1246/cl.2005.638
- Mukaiyama, T.; Ikegai, K.; Aoki, H. Proc. Japan Acad. 2005, 81, 103-109. https://doi.org/10.2183/pjab.81.103
- Mukaiyama, T.; Ikegai, K. Chem. Lett. 2004, 33, 1522-1523. https://doi.org/10.1246/cl.2004.1522
- Mukaiyama, T.; Masutani, K.; Hagiwara, Y. Chem. Lett. 2004, 33, 1192-1193. https://doi.org/10.1246/cl.2004.1192
- Ranu, B. C.; Mandal, T. J. Org. Chem. 2004, 69, 5793-5795. https://doi.org/10.1021/jo0493727
- Kumar, R.; Mabrouk, H. E.; Tuck, D. G. J. Chem Soc. Dalton Trans. 1998, 1045.
- Tu, Z.; Lin, C.; Jang, Y.; Jang, Y. J.; Ko, S.; Fang, H.; Liu, J. T.; Yao, C. F. Tetrahedron Lett. 2006, 47, 6133-6137. https://doi.org/10.1016/j.tetlet.2006.06.061
Cited by
- ChemInform Abstract: A Mild and Efficient Method for Preparing Alkyl Phenyl Selenides from Alkyl Diphenyl Phosphinites. vol.42, pp.43, 2011, https://doi.org/10.1002/chin.201143174
- The design of redox active thiol peroxidase mimics: Dihydrolipoic acid recognition correlates with cytotoxicity and prooxidant action vol.104, pp.None, 2016, https://doi.org/10.1016/j.bcp.2016.01.012