Organic sulfur compounds. VIII. Addition of thiols to conjugated diolefins
AA Oswald, K Griesbaum, WA Thaler…
Index: Oswald,A.A. et al. Journal of the American Chemical Society, 1962 , vol. 84, p. 3897 - 3904
Full Text: HTML
Citation Number: 69
Abstract
Addition of ionic and free radical reagents to conjugated dienes usually gives rise to both normal 1, Z-addition and 1, 4-conjugate addition. Kharasch and co-workers reported about a quarter of a century ago 3, 4 that in the presence of peroxides the addition of hydrogen bromide and hydrogen chloride to butadiene resulted predominantly in 1, 4-adducts while in the absence of peroxides mainly the 1, 2-adducts were formed. Carbon tetrachloride and ...
Related Articles:
[Cere, Vanda; Massaccesi, Franco; Pollicino, Salvatore; Ricci, Alfredo Synthetic Communications, 1996 , vol. 26, # 5 p. 899 - 907]
[Komine, Nobuyuki; Sako, Akari; Hirahara, Shin-Ya; Hirano, Masafumi; Komiya, Sanshiro Chemistry Letters, 2005 , vol. 34, # 2 p. 246 - 247]
[Bach, Thorsten; Koerber, Christina Journal of Organic Chemistry, 2000 , vol. 65, # 8 p. 2358 - 2367]
[Cere, Vanda; Massaccesi, Franco; Pollicino, Salvatore; Ricci, Alfredo Synthetic Communications, 1996 , vol. 26, # 5 p. 899 - 907]
[Cere, Vanda; Massaccesi, Franco; Pollicino, Salvatore; Ricci, Alfredo Synthetic Communications, 1996 , vol. 26, # 5 p. 899 - 907]