Samarium (II) iodide-mediated deoxygenative debromination of α-bromo-β-hydroxy (acetoxy) phenyl sulfones: synthesis of α, β-unsaturated sulfones
V Reutrakul, S Jarussophon, M Pohmakotr…
Index: Reutrakul, Vichai; Jarussophon, Suwatchai; Pohmakotr, Manat; Chaiyasut, Yupa; U-Thet, Saengvimon; Tuchinda, Patoomratana Tetrahedron Letters, 2002 , vol. 43, # 12 p. 2285 - 2288
Full Text: HTML
Citation Number: 7
Abstract
Deoxygenative debromination of α-bromo-β-hydroxy (acetoxy) phenyl sulfones with samarium (II) iodide led to substituted α, β-unsaturated sulfones in good to excellent yields. The E-isomer is the major product. A possible mechanism via an α-sulfonyl radical pathway is proposed.
Related Articles:
[Wnuk, Stanislaw F.; Garcia Jr., Pedro I.; Wang, Zhizhong Organic Letters, 2004 , vol. 6, # 12 p. 2047 - 2049]
[Palomo, Claudio; Aizpurua, Jesus M.; Garcia, Jesus M.; Ganboa, Inaki; Cossio, F. P.; et al. Journal of Organic Chemistry, 1990 , vol. 55, # 8 p. 2498 - 2503]
[Baba, Yoko; Toshimitsu, Akio; Matsubara, Seijiro Chemistry Letters, 2007 , vol. 36, # 7 p. 864 - 865]
[Reutrakul, Vichai; Panyachotipun, Chitchanun; Hahnvajanawong, Viwat; Sotheeswaran, S. Tetrahedron Letters, 1984 , vol. 25, # 17 p. 1825 - 1828]
[Reutrakul, Vichai; Panyachotipun, Chitchanun; Hahnvajanawong, Viwat; Sotheeswaran, S. Tetrahedron Letters, 1984 , vol. 25, # 17 p. 1825 - 1828]