Stereoselective synthesis of alkenes and alkenyl sulfides from alkenyl halides using palladium and ruthenium catalysts
S Murahashi, M Yamamura…
Index: Murahashi,S.-I. et al. Journal of Organic Chemistry, 1979 , vol. 44, # 14 p. 2408 - 2417
Full Text: HTML
Citation Number: 303
Abstract
Alkenyl halides react with organolithium compounds, such as alkyl, aryl, and heterocyclic lithiums, in the presence of zerovalent palladium compounds to form alkenes stereoselectively under both stoichiometric and catalytic conditions. Alkenyl halides also are easily converted to the corresponding alkenyl sulfides stereoselectively upon treatment with thiolate anions in the presence of the same palladium catalyst. These reactions occur ...
Related Articles:
[Bi, Yubai; Neckers, Douglas C. Tetrahedron Letters, 1992 , vol. 33, # 9 p. 1139 - 1142]
[Bi, Yubai; Neckers, Douglas C. Tetrahedron Letters, 1992 , vol. 33, # 9 p. 1139 - 1142]