Michael type addition of halides to alkynyl (phenyl) iodonium tetrafluoroborates. Stereoselective synthesis of (Z)-β-halovinyl (phenyl) iodonium halides
…, K Uemura, K Oshima, Y Masaki, M Kunishima, S Tani
Index: Ochiai, Masahito; Uemura, Koji; Oshima, Kunio; Masaki, Yukio; Kunishima, Munetaka; Tani, Shohei Tetrahedron Letters, 1991 , vol. 32, # 36 p. 4753 - 4756
Full Text: HTML
Citation Number: 26
Abstract
Abstract Michael type addition of halide ions (Cl− and Br−) to alkynyl (phenyl)-iodonium tetrafluoroborates (1) under acidic conditions proceeds in a completely stereoselective manner and affords (Z)-β-halovinyl (phenyl) iodonium halides (2), potential progenitors for generating α-haloalkylidenecarbenes, in high yields.
Related Articles:
[Oda, Hiroji; Oshima, Koichiro; Nozaki, Hitosi Chemistry Letters, 1985 , p. 53 - 56]
[Ochiai, Masahito; Tsuchimoto, Yoshimi; Hayashi, Takanori Tetrahedron Letters, 2003 , vol. 44, # 29 p. 5381 - 5384]