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Cyclization halopalladation

B.ii. Halopalladation-Initiated Carbonylative Cyclization of Yndiols to /8-Chloro-y-butenolides... [Pg.623]

As discussed in Sect. V.3.5, halide ions can also add to the palladium 7r-complexes, and the process may be termed halopalladation. Addition of Pd and a halogen, such as Cl and Br, to olefins, acetylenes, allenes, and conjugated dienes has been reported. However, most of the currently useful reactions initiated by halopalladation involve the use of alkynes as the substrates. Halopalladation of aUcynes gives vinylpalladium intermediates, which can undergo intramolecular carbopalladation to form cyclized products. Pd-catalyzed cyclization of ally lie aUcynoates can produce 7r-alkylidene-y-butyrolactones, which represent a basic structural unit in a wide variety of biologically active natural products. [Pg.655]


See other pages where Cyclization halopalladation is mentioned: [Pg.380]    [Pg.630]    [Pg.632]    [Pg.632]   


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Halopalladation

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