References
- Carreno, M. C. Chem. Rev. 1995, 95, 1717. https://doi.org/10.1021/cr00038a002
- Solladie, G. Synthesis 1981, 185.
- Madesclaire, M. Tetrahedron 1988, 44, 6537. https://doi.org/10.1016/S0040-4020(01)90096-1
- Drabowicz, J.; Togo, H.; Mikolajczyk, M.; Oae, S. Org. Prep. Proc. Int. 1984, 16, 171. https://doi.org/10.1080/00304948409355456
- Schmizu, M.; Shibuya, K.; Hayakawa, R. Synlett 2000, 1437.
- Khurana, J. M. Tetrahedron Lett. 1998, 39, 3829. https://doi.org/10.1016/S0040-4039(98)00623-6
- Yadav, J. S.; Reddy, B. V. S.; Srinivas, C.; Srihari, P. Synlett 2001, 854.
- Balicki, R. Synthesis 1991, 155.
- Miller, S. J.; Collier, T. R.; Wu, W. Tetrahedron Lett. 2000, 41, 3781. https://doi.org/10.1016/S0040-4039(00)00502-5
- Balicki, R. Synthesis 1991, 155.
- Firouzabadi, H; Iranpoor, N.; Jafarpour, M. J. Sulfur Chem. 2005, 26, 313. https://doi.org/10.1080/17415990500395624
- Olah, G. A.; Narang, S. C.; Gupta, B. G. B.; Malhotra, R. Synthesis 1979, 61.
- Bahrami, K.; Khodaei, M. M.; Karimi, A. Synthesis 2008, 2543.
- Cintas, D. Activated Metals in Organic Synthesis; CRC: Boca Raton, 1993.
- Balicki, R. Synthesis 1991, 155.
- Drabowicz, J.; Mikorajczyk, M. Synthesis 1976, 527.
- Oh, K. S.; William, E. K. Tetrahedron 2009, 65, 2966. https://doi.org/10.1016/j.tet.2009.02.013
- Yadav, J. S.; Ganganna, B.; Bhunia, D. C.; Srihari, P. Tetrahedron Lett. 2009, 50, 4318. https://doi.org/10.1016/j.tetlet.2009.03.171
- Wang, R.; Li, B. G.; Huang, T. K.; Shi, L.; Lu, X. X. Tetrahedron Lett. 2007, 48, 2071. https://doi.org/10.1016/j.tetlet.2007.01.142
- Ravikumar, P. C.; Yao, L. H.; Fleming, F. F. J. Org. Chem. 2009, 74, 7294. https://doi.org/10.1021/jo901287f
- Hou, J. T.; Liu, Y. H.; Zhang, Z. H. J. Heterocycl. Chem. 2010, 47, 703.
- Yoo, B. W.; Choi, K. H.; Lee, S. J.; Yoon, C. M.; Kim, S. H.; Kim, J. H. Synth. Commun. 2002, 32, 63. https://doi.org/10.1081/SCC-120001509
- Yoo, B. W.; Lee, S. J.; Yoo, B. S.; Choi, K. I.; Kim, J. H. Synth. Commun. 2002, 32, 2489. https://doi.org/10.1081/SCC-120003398
- Yoo, B. W.; Choi, K. H.; Kim, D. Y.; Choi, K. I.; Kim, J. H. Synth. Commun. 2003, 33, 53. https://doi.org/10.1081/SCC-120015558
- Yoo, B. W.; Park, M. C.; Shin, J. I. Bull. Korean Chem. Soc. 2009, 30, 1927. https://doi.org/10.5012/bkcs.2009.30.9.1927
- Yoo, B. W.; Kim, J. H.; Yang, M. H. Bull. Korean Chem. Soc. 2010, 31, 791. https://doi.org/10.5012/bkcs.2010.31.04.791
- Yoo, B. W.; Kim, S. H.; Kim, J. H. Bull. Korean Chem. Soc. 2010, 31, 2757. https://doi.org/10.5012/bkcs.2010.31.10.2757
- Sarmah, B. K.; Barua, N. C. Tetrahedron 1991, 47, 8587. https://doi.org/10.1016/S0040-4020(01)82402-9
- Bezbarua, M. S.; Bez, G.; Barua, N. C. Chem. Lett. 1999, 325.
- Wang, W. B.; Shi, L. L.; Huang, Y. Z. Tetrahedron Lett. 1990, 31, 1185. https://doi.org/10.1016/S0040-4039(00)88759-6
- Barua, M.; Boruah, A.; Prajapati, D.; Sandhu, J. S. Tetrahedron Lett. 1996, 37, 4559. https://doi.org/10.1016/0040-4039(96)00844-1
- B. Rama, R.; Gitali, D.; Yoofisaca, S. N.; Anil, K. S. Synlett 2005, 358.
- Alper, H.; Kenney, E. C. H. Tetrahedron Lett. 1970, 11, 53. https://doi.org/10.1016/S0040-4039(01)87563-8
- Chasar, D. W. J. Org. Chem. 1971, 36, 613. https://doi.org/10.1021/jo00803a033
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