Palladium-Catalyzed Intermolecular Three-Component Coupling of Organic Halides with Alkynes and Alkenes: Efficient Synthesis of Oligoene Compounds
作者:Kana Shibata、Tetsuya Satoh、Masahiro Miura
DOI:10.1002/adsc.200700171
日期:2007.10.8
intermolecular three-componentcoupling of aryl or vinyl halides, diarylacetylenes, and monosubstituted alkenes effectively proceeds in the presence of palladium acetate, lithium chloride, and sodium bicarbonate as catalyst, promoter, and base, respectively, in aqueous DMF or DMSO to produce the corresponding 1,3-butadiene or 1,3,5-hexatriene derivatives. Use of dienyl bromides allows the coupling to afford
The photolysis of 1 produces the carbene 2, which is transformed into the short lived phosphene 4 by phenyl migration. With the α, β-unsaturated ketones 6a–d in a [2+2] cycloaddition 4 yields the 1,2λ5-oxaphos-phetanes 7a–d The heterocycles partially undergo a photofragmentation, which produces the olefines 9a–d and the heterocumulene 8. If 4 is generated from 1 under thermal conditions in the presence
Palladium-Catalyzed Intermolecular Three-Component Coupling of Aryl Iodides, Alkynes, and Alkenes To Produce 1,3-Butadiene Derivatives
作者:Kana Shibata、Tetsuya Satoh、Masahiro Miura
DOI:10.1021/ol0503743
日期:2005.4.1
[reaction: see text] The sequential three-componentcoupling of aryl iodides, diarylacetylenes, and monosubstituted alkenes effectively proceeds in the presence of Pd(OAc)(2), LiCl, and NaHCO(3) as catalyst, promoter, and base, respectively, in DMF-H(2)O to produce the corresponding 1,3-butadiene derivatives.