Palladium-catalyzed cross-coupling of perfluoroalkenylzinc reagents with aryl iodides. A new, simple synthesis of .alpha.,.beta.,.beta.-trifluorostyrenes and the stereoselective preparation of 1-arylperfluoropropenes
Palladium catalyzed coupling of F-cinyl zinc reagents with aryl iodides. An improved synthesis of α,β,β-trifluorostyrenes and the stereospecific preparation of 1-phenyl-F-propenes
作者:Pamela L. Heinze、Donald J. Burton
DOI:10.1016/s0022-1139(00)85092-7
日期:1986.2
provides a practical high yield route to α,β,β- trifluorostyrenes. Ortho, meta, and para substituted aryl iodides all work equally well. Similar coupling with - and -1-iodo--propenes outlines the first stereospecific preparative route to 1-aryl--olefins. This approach provides a rapid, easily scaled-up synthesis a one pot procedure to these valuable styrenes from commercially available precursors without
SOROKINA, R. S.;RYBAKOVA, L. F.;KALINOVSKIJ, N. O.;BELETSKAYA, I. P., IZV. AN CCCP. CEP. XIM., 1985, N 7, 1647-1649
作者:SOROKINA, R. S.、RYBAKOVA, L. F.、KALINOVSKIJ, N. O.、BELETSKAYA, I. P.
DOI:——
日期:——
HEINZE, PAMELA L.;BURTON, DONALD J., J. ORG. CHEM., 53,(1988) N 12, 2714-2720
作者:HEINZE, PAMELA L.、BURTON, DONALD J.
DOI:——
日期:——
Palladium-catalyzed cross-coupling of perfluoroalkenylzinc reagents with aryl iodides. A new, simple synthesis of .alpha.,.beta.,.beta.-trifluorostyrenes and the stereoselective preparation of 1-arylperfluoropropenes