Reductive Bromine Atom-Transfer Reaction
S Sumino, A Fusano, I Ryu
Index: Sumino, Shuhei; Fusano, Akira; Ryu, Ilhyong Organic Letters, 2013 , vol. 15, # 11 p. 2826 - 2829
Full Text: HTML
Citation Number: 5
Abstract
Atom-transfer radical (ATR) reactions of alkenes with R–X usually give products having new C–C and C–X bonds at the adjacent carbons. However, when the reaction was carried out under irradiation using a low-pressure Hg lamp, addition/reduction products were obtained in good yield. Hydrogen bromide, formed by H-abstraction of a bromine radical from alkenes, is likely to play a key role in the reductive ATR reaction.
Related Articles:
[Baarschers, Willem Hendrik; Li, Maria Angela Canadian Journal of Chemistry, 1983 , vol. 61, p. 1784 - 1787]
[Shevchenko; Volynskii Petroleum Chemistry, 2008 , vol. 48, # 2 p. 123 - 128]
[Dox Journal of the American Chemical Society, 1924 , vol. 46, p. 1709]
[Dox Journal of the American Chemical Society, 1924 , vol. 46, p. 1709]
[Bertz, Steven H.; Dabbagh, Gary Journal of Organic Chemistry, 1984 , vol. 49, p. 1119 - 1122]